All Recalls

95,102 total recalls in our database

cGMP Deviations: This recall is a result of the original manufacturer's recall, in which the firm did not adequately investigate customer complaints.

Apr 29, 2015 Prescription Drugs Nationwide View Details β†’

cGMP Deviations: This recall is a result of the original manufacturer's recall, in which the firm did not adequately investigate customer complaints.

Apr 29, 2015 Prescription Drugs Nationwide View Details β†’

A product complaint was received stating that a carton labeled as a Precoat Stemmed Tibia Size 3 was opened for use and the contents were a non-augmented Stemmed Tibia Plate size 3.

Dec 3, 2015 Implants & Prosthetics View Details β†’

Stability data does not substantiate the labeled two-year shelf life of affected product.

Dec 3, 2015 Infusion Pumps Nationwide View Details β†’

Product mislabeled as latex free. Actual Catalog number 1581, lot 2020-10AN. contains latex. This could pose a health risk to users with sensitivity or allergic reaction to latex, which could range from mild to severe.

Dec 1, 2015 Implants & Prosthetics Nationwide View Details β†’