Complete FDA and NHTSA recall records dated in July 2018.
These records include useful source details for the selected month.
The manufacturer has discovered that potentially out-of-specification products may have left the factory. Non-conforming cannulation of the nails may result in reduced component strength…
The firm was notified by their customer that the product test positive for Salmonella
Del Monte has recalled the products because they may be linked to this recent cluster of illnesses and have the potential to be contaminated with Cyclospora
During a FDA foreign inspection, it was found that four products did not declare allergens.
Honey Mama's Oregon Peppermint Cacao-Nectar Bar, 2.5 oz, is recalled due to undeclared almonds.
The firm was notified by their customer that the product test positive for Salmonella
During a FDA foreign inspection, it was found that four products did not declare allergens.
Brew Dr. Kombucha US Clear Mind, 32 oz bottles, is recalled because glass fragments were found inside the bottle.
Del Monte has recalled the products because they may be linked to this recent cluster of illnesses and have the potential to be contaminated with Cyclospora
Vanilla ice cream not labeled for individual sale was distributed to stores for individual sale. They are therefore missing a nutrition facts panel, an ingredients statement , and they do…
During a FDA foreign inspection, it was found that four products did not declare allergens.
The recall was initiated after learning from a retail customer that a limited number of bottles were mislabeled. The product contains milk and egg not declared on the bottle.
The product may contain small metal pieces (approximately 2 mm to 8 mm) from a sifter screen.
During a FDA foreign inspection, it was found that four products did not declare allergens.
Sparkling ICE Cherry Limeade, 17 oz. bottles, is recalled after the firm received a small number of customer complaints that reported an off-taste and off-odor of the product.
Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella contamination
CGMP Deviations: Syringes were filled with 19mL of potassium chloride when the labels displayed a fill of 20mL.
Failed Impurities and Degradation Specifications and Subpotent Drug: out-of-specification (OOS) test results for below assay and above specification for degradants.
Temperature Abuse: Product samples of Admelog may not have been shipped at proper temperature.
CGMP Deviations: The manufacturer of this product recalled because they were not manufactured under current good manufacturing practices.
Presence of Particulate Matter: identified as glass and silicone material
Failed Impurities/Degradation Specification; out-of-specification results for the Enalapril DKT degradant
Subpotent Drug: Stability data does not support the current expiration dating of 55 days after compounding.
There is a potential for imprecise results when using the slides. Increase in imprecision when using PHYT coating 0165. This leads to higher and lower than expected results for both quality…
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.
