Complete FDA and NHTSA recall records dated in February 2017.
These records include useful source details for the selected month.
The firm expanded recall to include additional batches. Product recalled because of off odor and taste due to microbial contamination.
The firm expanded recall to include additional batches. Product recalled because of off odor and taste due to microbial contamination.
The product may contain undeclared walnuts from intermediate layer cake supplier.
Mann Packing was notified by a customer that the incorrect bottom label is on their Organic Veggie Tray with Best By date of January 14, 2017 and does not declare the allergens of egg,…
Product quality issue. Through sampling, FDA revealed the presence of non-pathogenic Gram Positive Rods (microorganisms).
The firm expanded recall to include additional batches. Product recalled because of off odor and taste due to microbial contamination.
Product contains undeclared peanuts
The firm expanded recall to include additional batches. Product recalled because of off odor and taste due to microbial contamination.
The firm was notified by their contract manufacturer that they received ingredients that may be contaminated with Salmonella.
Del Dee Foods, Inc.withdrew Lot# PP33116-0-D after receiving a report of salmonella found in two sample tests taken from product in the above lot before it reached the consumer.
Basil Pesto ingredient list did not list "milk" after the ingredient Parmesan Cheese.
The firm expanded recall to include additional batches. Product recalled because of off odor and taste due to microbial contamination.
Back label of Lobster Bisque product was mislabeled as Butternut Squash Soup (which contains fewer allergens [only milk] than the Lobster Bisque [milk, shellfish, wheat])
In response to a consumer complaint, Investigation by the manufacturer determined that a partial black rat was found in the product.
The product may contain undeclared walnuts from intermediate layer cake supplier.
The product may contain undeclared walnuts from intermediate layer cake supplier.
Failed Dissolution Specifications
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Failed Tablet/Capsule Specification: Tablets were found to be twice the thickness in one lot of product.
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Subpotent Drug
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
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.
