Complete FDA and NHTSA recall records dated in 2018, 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.
The set screw is not able to advance or reverse from the original position in the nail.
The slides do not meet the maximum allowable interference (MAI) claims for triglyceride interference when using serum samples. Triglyceride interference on the Cl- Slide was observed around…
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The set screw is not able to advance or reverse from the original position in the nail.
The product may be contaminated with Listeria monocytogenes.
Product contains undeclared allergens, egg, crustacean, and pork.
Product contains undeclared allergens egg and crustacean.
Potential for cleaning chemical introduced into product due to process deviation while cleaning pasteurizer.
During FDA foreign inspection of manufacturer, it was discovered that milk, wheat and soy were not declared as sub ingredients or in the allergen statement
During FDA foreign inspection of manufacturer, it was discovered that milk, wheat and soy were not declared as sub ingredients or in the allergen statement
The firm was notified by a customer that mold was in the product.
Defective Delivery System: Water ingress through the lower water cup sensor of the device.
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.
