Canteen Inc. dba MG Foods FRESH TO YOU Deluxe Club Wrap, Net Wt recall — FDA F-0421-2021
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
Complete FDA and NHTSA recall records dated in April 2021.
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The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
Potential Salmonella contamination
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
The firm recieved consumer complaints of premature spoilage of the refrigerated gravy product.
Vitamin D3 stability sample analyzed and found to be less than 100% of label claim.
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
Cross Contamination with Other Product: Product is being recalled due to Trace Amounts of Quetiapine Fumarate
Labeling; Label Mix-up; some bottles containing Foam Skin Cleanser soap are incorrectly labeled as Moisturizing Foam Hand Sanitizer
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
Failed Moisture Limits: Out of specification for water content
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A small percentage of implanted cardiac devices, from a well-defined subset, may experience a shortened Recommended Replacement Time (RRT) to End of Service (EOS) interval following an…
Potential for system to produce falsely elevated parathyroid hormone (PTH) results from patient samples.
Two lots of test strips failed QC testing using blank buffer due to false positives.
Their is a potential that the automated staining instrument with software version 3.5.3.1 may move with random speeds in random direction across its range of motion. This could result in…
Customers are being notified of results from a Toxicological Risk Assessment related to potential for aluminum ions to leach into warmed fluids.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.