Mann Packing Company 2 lb bags recall — FDA F-0172-2018
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
Complete FDA and NHTSA recall records dated in 2017, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
Ingredients statement declared whey, powdered cheese and cheddar cheese but did not declare milk. In addition, FD&C colors Yellow #5 and Yellow #6 are not declared.
Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
Date coding ink was being printed directly on the food contact surface of packaging, allowing the ink to be in direct contact with the product. The ink is not approved for food use.
Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
Date coding ink was being printed directly on the food contact surface of packaging, allowing the ink to be in direct contact with the product. The ink is not approved for food use.
Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
Recall of four varieties of Probiotic drinks due to premature spoilage. Testing has identified Candida lusitaniae as the predominate microorganism as the cause of spoilage.
Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
Date coding ink was being printed directly on the food contact surface of packaging, allowing the ink to be in direct contact with the product. The ink is not approved for food use.
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
Date coding ink was being printed directly on the food contact surface of packaging, allowing the ink to be in direct contact with the product. The ink is not approved for food use.
Date coding ink was being printed directly on the food contact surface of packaging, allowing the ink to be in direct contact with the product. The ink is not approved for food use.
On 10/30/2017, Giant Eagle received notice from their contract manufacturer to recall Market District Coffee Beans Covered in Dark Chocolate due to undeclared milk in the dark chocolate.…
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
Date coding ink was being printed directly on the food contact surface of packaging, allowing the ink to be in direct contact with the product. The ink is not approved for food use.
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.