Shelf Stable Meal Request Form
Shelf Stable Meal Request Form
RECALL: Macgregors Meat and Seafood Ltd, Ready-to-Eat Pork Products
Dear Partners,
Please review the following recall below, check your inventory for affected products, and take necessary action.
Post this recall notice where those accessing your organization can see it (e.g., bulletin board, website, social media).
If you are not the most appropriate person to receive this notice, please forward this communication to the responsible representative at your organization. To ensure recalls are sent to the appropriate person in the future, feel free to respond to this email with other email addresses that should receive them.
Let us know if you have any questions or concerns.
___________________________________________________________________
Macgregors Meat and Seafood Ltd, a Woodbridge, Ontario, Canada establishment, is recalling approximately 2,745 pounds of frozen, ready-to-eat pork products that were not presented for import reinspection into the United States, the U.S. Department of Agriculture ‘s Food Safety and Inspection Service (FSIS) announced today.
The following products are subject to recall [view labels]:
- 1.5-lb. cartons containing “44TH Street Slow Cooked BABY BACK RIBS MAPLEWOOD SMOKED SAUCE” with Julian dates 3453 and 0154 printed on the side of the immediate package. The product is packed in cases marked with Cert. No. Cert 043436, Production Date 3453 with USE BY 2024 DE 10 and Production Date 0154 with USE BY 2025 JA 14.
- 1.5-lb. cartons containing “44TH Street Glazed, Slow Cooked BABY BACK RIBS HONEY GARLIC SAUCE” with Julian dates 1453 and 1593 printed on the side of the immediate package. The product is packed in cases marked with Cert. No. Cert 043436, Production Date 1453 with USE BY 2024 MA 24 and Production Date 1593 with USE BY 2024 JN 07.
The products subject to recall bear Canadian establishment number 566 printed inside the Canadian inspection mark located on the label. These items were shipped to retail locations and restaurants in Indiana, Kentucky, Michigan, New York, Ohio, and Pennsylvania.
The problem was discovered when the firm notified FSIS that the product was not presented for FSIS import reinspection.
There have been no confirmed reports of illness or adverse reactions due to consumption of these products. Anyone concerned about an illness or reaction should contact a healthcare provider.
FSIS is concerned that some product may be in consumer and restaurant freezers. Consumers who have purchased these products are urged not to consume them. Restaurants are urged not to serve these products. The products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Duncan Macgregor, Jr., General Manager, Macgregors Meat & Seafood Ltd, at 416-749-5951, extension 205, or duncanjr@macgregors.com.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.
Product Images
RECALL: Additional Quaker Items
Dear Partners,
Please review the following recall below, check your inventory for affected products, and take necessary action.
Post this recall notice where those accessing your organization can see it (e.g., bulletin board, website, social media).
If you are not the most appropriate person to receive this notice, please forward this communication to the responsible representative at your organization. To ensure recalls are sent to the appropriate person in the future, feel free to respond to this email with other email addresses that should receive them.
Let us know if you have any questions or concerns.
_____________________________________________________________
January 31, 2024 – An additional granola bar has been added to the U.S. Recalled Products list as indicated on the first row of the chart below. This product was discontinued in September 2023 and has “Best Before” dates of February 10 or 11, 2024. Consumers should check their pantries and dispose of the product.
A previous press release was issued on 12/15/2023.
CHICAGO, Illinois – January 11, 2024 – The Quaker Oats Company today announced an expansion of the December 15, 2023, recall to include additional cereals, bars and snacks listed below because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
The products listed below are sold throughout the 50 United States, Puerto Rico, Guam and Saipan. Consumers should check their pantries for any of the products listed below and dispose of them. Additionally, consumers with any product noted below can contact Quaker Consumer Relations (9 a.m. – 4:30 p.m. CST, Mon.-Fri.) at 1-800-492-9322 or visit www.QuakerRecallUSA.comExternal Link Disclaimer for additional information or product reimbursement.
Consumers can scan the SmartLabel QR code on the product package to determine if it has been recalled.
Quaker has informed the FDA of our actions.
This recall applies to the specific products listed below, in addition to the products announced on December 15, 2023. A combined list of recalled products is available on www.QuakerRecallUSA.com External Link Disclaimer.
_________________________________________________
Additional Products:
On January 11, 2024 the Quaker Oats Company announced an expansion of the recall to include additional cereals and bars.
This recall includes Quaker Chewy Granola Bars and Cereals, Cap’n Crunch Bars and select Cereals, Gamesa Marias Cereal, Gatorade Peanut Butter Chocolate Protein Bars, Munchies Munch Mix and Snack Boxes that include these products.
For a detailed list, including UPC, product name, and product image, please click on the category below.
- Gamesa Marias Cereal
- Gatorade Protein Peanut Butter Chocolate Bars
- Munchies Mix Munch Mix
- Snack Boxes
This recall does not include:
- Quaker Oats
- Quaker Instant Oats
- Quaker Grits
- Quaker Oat Bran
- Quaker Oat Flour
- Quaker Rice Snacks
RECALL: Truong Giang Distributor Corp Issues Allergy Alert on Undeclared Sulfites in Dried Mango
Dear Partners,
Please review the following recall below, check your inventory for affected products, and take necessary action.
Post this recall notice where those accessing your organization can see it (e.g., bulletin board, website, social media).
If you are not the most appropriate person to receive this notice, please forward this communication to the responsible representative at your organization. To ensure recalls are sent to the appropriate person in the future, feel free to respond to this email with other email addresses that should receive them.
Let us know if you have any questions or concerns.
Company Announcement
TRUONG GIANG DISTRIBUTOR CORP of Philadelphia, PA is recalling Golden Owl Dried Mango, because it may contain undeclared sulfites. People who have an allergy or severe sensitivity to sulfites run the risk of serious or life-threatening allergic reaction if they consume these products.
Product was distributed nationwide in retail stores.
This product is packaged in 7 oz (100g) clear plastic containers with UPC 816710-024461 located on the left side of the container.
No illnesses have been reported to date.
The recall was initiated after routine sampling by the New York State Department of Agriculture and Markets found sulfites in the product which was distributed in packaging that did not reveal the presence of sulfites. Subsequent investigation indicates the problem was caused by a temporary breakdown in the supplier’s labeling processes.
Consumers who have purchased the product are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 215-456-1883 Monday to Friday 8AM to 5PM EST.
Company Contact Information
Consumers:
TRUONG GIANG DISTRIBUTOR CORP
215-456-1883
Product Photos
RECALL: Robitussin Honey CF Max Day and Nighttime Adult Cough Medicine
Dear Partners:
Please review the following recall below, check your inventory for affected products, and take necessary action.
Post this recall notice where those accessing your organization can see it (e.g., bulletin board, website, social media).
If you are not the appropriate person to receive this notice, please contact Dare to Care to update the contact information needed for this email.
Let us know if you have any questions or concerns.
___________________________________________________________________
Haleon is voluntarily recalling eight lots of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult to the consumer level. The product is being recalled due to microbial contamination.
In immunocompromised individuals, the use of the affected product could potentially result in severe or life-threatening adverse events such as fungemia or disseminated fungal infection. In non-immunocompromised consumers, the population most likely to use the product, life-threatening infections are not likely to occur. However, the occurrence of an infection that may necessitate medical intervention cannot be completely ruled out.
To date, Haleon has not received any reports of adverse events related to this recall.
Robitussin Honey CF Max Day and Nighttime are cough syrups indicated for the temporary relief of symptoms occurring with cold or flu, hay fever, or other respiratory allergies. This recall covers only the following lots:
Product | Lot Number | Expiry Date |
ROBITUSSIN HONEY CF MAX DAY ADULT 4OZ | T10810 | 31OCT2025 |
ROBITUSSIN HONEY CF MAX DAY ADULT 8OZ | T08730 T08731 T08732 T08733 T10808 | 31MAY2025 31MAY2025 31MAY2025 31MAY2025 30SEP2025 |
ROBITUSSIN HONEY CF MAX NT ADULT 8OZ | T08740 T08742 | 30JUN2026 30JUN2026 |
Haleon is notifying its distributors and customers directly and has provided them with instructions for the return of all recalled products. Consumers that have purchased the product listed should stop consumption immediately. Please call our Consumer Relations team at +1-800-245-1040 (Monday through Friday 8 AM to 6 PM Eastern Time) or reach out via email to mystory.us@haleon.com.
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
- Complete and submit the report Online: www.fda.gov/medwatch/report.htm
- Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
RECALL: Whitley’s Peanut Factory Issues an Allergy Alert on Undeclared Peanuts, Milk, Soy, Wheat, and Sesame for Limited Units of Deluxe Nut Mix 12oz (340g)
Dear Partners,
Please review the following recall below, check your inventory for affected products, and take necessary action.
Post this recall notice where those accessing your organization can see it (e.g., bulletin board, website, social media).
If you are not the most appropriate person to receive this notice, please forward this communication to the responsible representative at your organization. To ensure recalls are sent to the appropriate person in the future, feel free to respond to this email with other email addresses that should receive them.
Let us know if you have any questions or concerns.
Company Announcement
Whitley’s Peanut Factory of Hayes, Virginia is recalling 12oz Deluxe Nut Mix with specific code dates because they may contain undeclared peanuts, milk, soy, wheat, and sesame. People who have an allergy or severe sensitivity to these ingredients run the risk of serious or life-threatening allergic reaction if they consume these products.
Deluxe Nut Mix was distributed to wholesalers and retail customers nationwide between the weeks of August 21st, 2023 through January 10th, 2024. The product(s) were available for purchase on the company website at www.WhitleysPeanut.comExternal Link Disclaimer, through mail-order catalogue, and in select US retail stores.
The recall of this product was initiated after the Quality Assurance Department became aware of a limited number of 10.5oz Whit’s Party Mix tins labeled with 12oz Deluxe Nut Mix labels. The depth of the recall has been expanded to include the previous production date through the time in which the company became aware of the issue. While both products contain almonds, Whit’s Party Mix also includes peanuts, milk, soy, wheat, and sesame which are not listed in the “Contains” statement of the Deluxe Nut Mix label.
Recalled product can be easily identified by checking the manufacturing code on the bottom of the tin. Only 12oz Deluxe Nut Mix labeled tins bearing the code dates below are affected.
UPC Code | Description | Lot Code(s) |
Single Unit UPC: 703795000551 | Deluxe Nut Mix 12oz(340g) | MFG 22823; MFG 25023; MFG 25823; MFG 29323; MFG 35623 |
The company has received no reports of illness or injury to date.
Customers who may have purchased or received this product are advised to inspect any Deluxe Nut Mix 12oz tins for the lot codes above, and discontinue use immediately if found to be affected. Consumers may contact Customer Service for a refund, and safely dispose of any mislabeled tins. If a consumer experiences an allergic reaction, they are urged to seek medical attention right away. For questions, please contact CustomerCare@WhitleysPeanut.com, or call 1-800-470-2244 Monday through Friday, 8 AM to 5PM Eastern Time.
This recall is being executed with the knowledge of the US Food and Drug Administration
Company Contact Information
Consumers:
1-800-470-2244
CustomerCare@WhitleysPeanut.com
Product Photos
Company Announcement
Whitley’s Peanut Factory of Hayes, Virginia is recalling 12oz Deluxe Nut Mix with specific code dates because they may contain undeclared peanuts, milk, soy, wheat, and sesame. People who have an allergy or severe sensitivity to these ingredients run the risk of serious or life-threatening allergic reaction if they consume these products.
Deluxe Nut Mix was distributed to wholesalers and retail customers nationwide between the weeks of August 21st, 2023 through January 10th, 2024. The product(s) were available for purchase on the company website at www.WhitleysPeanut.comExternal Link Disclaimer, through mail-order catalogue, and in select US retail stores.
The recall of this product was initiated after the Quality Assurance Department became aware of a limited number of 10.5oz Whit’s Party Mix tins labeled with 12oz Deluxe Nut Mix labels. The depth of the recall has been expanded to include the previous production date through the time in which the company became aware of the issue. While both products contain almonds, Whit’s Party Mix also includes peanuts, milk, soy, wheat, and sesame which are not listed in the “Contains” statement of the Deluxe Nut Mix label.
Recalled product can be easily identified by checking the manufacturing code on the bottom of the tin. Only 12oz Deluxe Nut Mix labeled tins bearing the code dates below are affected.
UPC Code | Description | Lot Code(s) |
Single Unit UPC: 703795000551 | Deluxe Nut Mix 12oz(340g) | MFG 22823; MFG 25023; MFG 25823; MFG 29323; MFG 35623 |
The company has received no reports of illness or injury to date.
Customers who may have purchased or received this product are advised to inspect any Deluxe Nut Mix 12oz tins for the lot codes above, and discontinue use immediately if found to be affected. Consumers may contact Customer Service for a refund, and safely dispose of any mislabeled tins. If a consumer experiences an allergic reaction, they are urged to seek medical attention right away. For questions, please contact CustomerCare@WhitleysPeanut.com, or call 1-800-470-2244 Monday through Friday, 8 AM to 5PM Eastern Time.
This recall is being executed with the knowledge of the US Food and Drug Administration
Company Contact Information
Consumers:
1-800-470-2244
CustomerCare@WhitleysPeanut.com
Product Photos
RECALL: Rizo Lopez Food, Aged Cotija Mexican Grating Cheese
Dear Partners:
Please review the following recall below, check your inventory for affected products, and take necessary action.
Post this recall notice where those accessing your organization can see it (e.g., bulletin board, website, social media).
If you are not the appropriate person to receive this notice, please contact Dare to Care to update the contact information needed for this email.
Let us know if you have any questions or concerns.
_________________________________________________________________________
Rizo Lopez Foods, Inc. of Modesto, CA is recalling a total of 344 cases of Aged Cotija Mexican Grating Cheese (8oz), UPC 72724200043 batch number 4DW-23318 because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriage and stillbirths among pregnant women.
Aged Cotija Mexican Grating Cheese (8oz) was distributed nationwide through distributors.
The product comes in a small 8oz. “puck” shape wrapped in clear plastic marked with red and black lettering on the botom noted as “Cotija, made with Grade A Milk” along with an ingredient description. Nutritional facts are noted in black below the ingredient description. The top shows “Cotija Aged Mexican Grating Cheese” with orange background. Batch number is identified on the outer edge of the clear plastic with “SELL BY 05/12/24 BATCH 4DW-23318” in black lettering.
To date, no confirmed illnesses related to this product have been reported.
The recall was a result of a routine sampling program by the Hawaii State Department of Health’s Food and Drug Branch on Wednesday, January 3rd which revealed that the finished product contained the bacteria. Rizo Lopez Foods, Inc. has ceased the producon and distribution of the product as the FDA and Rizo Lopez Foods continue their investigation as to what caused the issue.
Consumers who have purchased Aged Cotija Mexican Grating Cheese (8oz). are urged to quarantine the product and destroy it. Consumers with questions may contact the company at 1-800-626-5587, Monday through Friday, 8:00am-5:00pm Pacific Standard Time.
####
Product Photos
RECALL: Frito Lay, Munchies Mix
Dear Partners:
Please review the following recall below, check your inventory for affected products, and take necessary action.
Post this recall notice where those accessing your organization can see it (e.g., bulletin board, website, social media).
If you are not the appropriate person to receive this notice, please contact Dare to Care to update the contact information needed for this email.
Let us know if you have any questions or concerns.
____________________________________________________________
RECALL: Quaker and Cap’n Crunch Bars
Dear Partners:
Please review the following recall below, check your inventory for affected products, and take necessary action.
Post this recall notice where those accessing your organization can see it (e.g., bulletin board, website, social media).
If you are not the appropriate person to receive this notice, please contact Dare to Care to update the contact information needed for this email.
Let us know if you have any questions or concerns.
__________________________________________________________________
For your information and action, Quaker and Cap’n Crunch Bars have been removed from Meijer shelves and are no longer available for sale due to: the potential to be contaminated with Salmonella.
UPC | UPC Description |
0-30000-00041-0 | QUAKER CHEWY YOGURT STRAWBERRY 1.23 OZ |
0-30000-00411-1 | CNC TREAT BAR CRUNCHBERRY KING 1.79 OZ |
0-30000-57278-8 | CNC TREAT BAR CRUNCHBERRY KING 1.79 OZ |
If you have received this product in your donations, please remove this item from your shelves immediately and destroy.
- « Previous Page
- 1
- 2
- 3
- 4
- 5
- …
- 61
- Next Page »