CGMP Deviations: Firm did not adequately investigate customer complaints.
All Recalls
95,114 total recalls in our database
CGMP Deviations: Firm did not adequately investigate customer complaints.
CGMP Deviations: Firm did not adequately investigate customer complaints.
CGMP Deviations: Firm did not adequately investigate customer complaints.
Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.
Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Adrucil (fluorouracil injection, USP) Pharmacy Bulk Package Not for Direct Infusion, 5 g/100 mL (50 mg/mL), For Intravenous Use Only, Rx Only, Teva Parenteral Medicines, Inc., Irvine, CA 92618, NDC 0703-3019-11
Teva Pharmaceuticals USA
Presence of Particulate Matter: Black particulate matter was identified as aggregate of silicone rubber pieces from a filler diaphragm and fluorouracil crystals.
Failed Content Uniformity Specifications: The product may not meet the limit for blend uniformity specification.
Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Subpotent Drug: menthol and methyl salicylate below specification
CORTISOL-MC, 10mg CAP, packaged in 30 and 90 count bottles, Rx Only, ABRAMS ROYAL pharmacy II, 4909 W Park Blvd, Suite 177, Plano, TX 75093 --- NDC 88888-0043-31
Abrams Royal Pharmacy II
Failed Content Uniformity Specifications: Failed Uniformity of Dosage Units specifications.
CGMP Deviations: Firm did not adequately investigate customer complaints.
Failed Content Uniformity Specifications: The product may not meet the limit for blend uniformity specification.
CGMP Deviations: Firm did not adequately investigate customer complaints.
Lima Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare
Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.
Integra LifeSciences Corp. d.b.a. Integra Pain Management Announces Voluntary Recall of Tuohy Needles (20 Gauge, 5 inch) due to incorrect packaging (labeled as 18 Gauge, 3. 5 inch).
Mississippi Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare
Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.
Arthroscopy Pack - contains Devon Light Glove Used during surgery
Stradis Healthcare
Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.
Philips GoSafe Communicator 7000L Personal emergency response system.
Lifeline Systems, Incorporated
Home communicator Model 7000L may not sense the phone line under certain unusual landline phone conditions.