Complete FDA and NHTSA recall records dated in April 2017.
These records include useful source details for the selected month.
Gerber Products Company is recalling Cheese Ravioli Gerber Pasta Pick-Ups because the egg allergen is missing from the "Contains" statement.
undeclared soy lecithin
J&J Distributing Company reported that a small amount of shred carrots were contaminated with metal pieces. The shred carrots were used as ingredient for other RTE items.
undeclared soy lecithin
Myers Cider Mill LLC, of Monroeville, Ohio has issued a voluntary recall of apple cider due to a process deviation.
undeclared soy lecithin.
undeclared soy lecithin and milk (cream and butter were declared).
J&J Distributing Company reported that a small amount of shred carrots were contaminated with metal pieces. The shred carrots were used as ingredient for other RTE items.
Product is recalled due to a potential contamination with E. coli O157:H7.
J&J Distributing Company reported that a small amount of shred carrots were contaminated with metal pieces. The shred carrots were used as ingredient for other RTE items.
During an FDA foreign inspection, it was discovered that Wheat was not properly declared on the product labeling. Wheat is an ingredient in the noodles contained in the product. Wheat is…
cGMP Deviations; manufacturer initiated recall of API product after deficiencies noted during a recent FDA inspection
Failed Impurities/Degradation Specifications: high out of specification results for one of the known degradation products, m-chlorobenzoic acid.
cGMP Deviations; manufacturer initiated recall of API product after deficiencies noted during a recent FDA inspection
Failed Tablet/Capsule Specifications; during an internal inspection, capsules were found with illegible print.
Failed Impurities/Degradation Specifications: high out of specification results for one of the known degradation products, m-chlorobenzoic acid.
cGMP Deviations; manufacturer initiated recall of API product after deficiencies noted during a recent FDA inspection
cGMP Deviations; manufacturer initiated recall of API product after deficiencies noted during a recent FDA inspection
Microbial Contamination of Non-Sterile Products: odor complaint of product due to microbial contamination.
Temperature Abuse: Certain pieces of these lots distributed by McKesson Medical Surgical Inc. were inadvertently stored refrigerated rather than the labeled room temperature recommendation.
Presence of Foreign Tablet/Capsule; Amoxicillin 500 mg was found in bottles of Penicillin V potassium 500 mg
Failed Impurities/Degradation Specifications: high out of specification results for one of the known degradation products, m-chlorobenzoic acid.
The firm was notified by their supplier that various cheese products test positive for Listeria monocytogenes.
Products contain undeclared wheat.
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.
