Product contains undeclared allergens egg and crustacean.
All Recalls
95,064 total recalls in our database
The product may be contaminated with Listeria monocytogenes.
Product contains undeclared allergens, egg, crustacean, and pork.
The product may be contaminated with Listeria monocytogenes.
Microbial Contamination of Non Sterile Products; Products contaminated with microoganisms, including but not limited to Staphylococcus saprophyticus and Burkholderia cepacia
Product Mix-Up: customer complaint that a sealed bottle labeled as Hydrochlorothiazide Tablets USP 12.5 mg contained only Spironolactone Tablets USP 25 mg.
Failed Impurities/Degradation Specifications; Out of specification stability testing results at the 18 month time point
Diltiazem HCl Extended-Release Capsules, USP 120 mg 100-count bottle, Rx only, Mylan Pharmaceuticals Inc. Morgantown, WV 26505. NDC 0378-5220-01
Mylan Pharmaceuticals
Failed Impurities/Degradation Specifications: Out of specification test results obtained during routine stability testing for related compound.
Microbial Contamination of Non Sterile Products; Products contaminated with microoganisms, including but not limited to Staphylococcus saprophyticus and Burkholderia cepacia
Presence of Precipitate: Customer complaint for visible precipitate in product believed to be the active ingredient furosemide.
Microbial Contamination of Non Sterile Products; Products contaminated with microoganisms, including but not limited to Staphylococcus saprophyticus and Burkholderia cepacia
Microbial Contamination of Non Sterile Products; Products contaminated with microoganisms, including but not limited to Staphylococcus saprophyticus and Burkholderia cepacia
Defective Delivery System: Water ingress through the lower water cup sensor of the device.
Diltiazem HCl Extended-Release Capsules, USP 120 mg 500-count bottle, Rx only, Mylan Pharmaceuticals Inc. Morgantown, WV 26505. NDC 0378-5220-05
Mylan Pharmaceuticals
Failed Impurities/Degradation Specifications: Out of specification test results obtained during routine stability testing for related compound.
Failed impurities/degradation specifications: Finished product contain a known product impurity about current specification levels.
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.
Edwards Lifesciences Avid Dual Stage Venous Drainage Cannula, 29/37F (9.6/12.3MM) X 37CM (14.5"), resterilized.
SPS Sterilization
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.