Product Recalls in Maine
Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,392 recalls have been distributed to Maine in the last 12 months.
Showing 22501–22520 of 48,770 recalls
Recalled Item: Valsartan Tablets USP 160 mg Recalled by American Health Packaging Due to...
The Issue: CGMP Deviation: Presence of NDEA (N-Nitrosodimethylamine), a carcinogen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Docetaxel Injection USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Defective Container: complaint for seal and cap vial issues that could lead...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FilmArray Gastrointestinal (GI) Panel Recalled by BioFire Diagnostics, LLC...
The Issue: Elevated rates of false positive results for Campylobacter and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMAGEnet 6 v1.53- IMAGEnet 6 Ophthalmic Data System is a Recalled by Topcon...
The Issue: When a patient is selected in the patient data and another patient is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaBeam Handpiece Recalled by PROCEPT BIOROBOTICS CORPORATION Due to...
The Issue: Certain lots may develop an internal leak due to a micro-crack in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEOPARD Miracle Honey packaged in a wooden box Recalled by USA LESS Inc. Due...
The Issue: Marketed Without An Approved NDA/ANDA: product tainted with undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by AVKARE Inc....
The Issue: CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP 50 mg 50 Tablets (5x10) Unit Dose boxes...
The Issue: CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by AVKARE Inc....
The Issue: CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fresenius Kabi CATSmart device (Continuous autotransfusion System). Labeled...
The Issue: Based on internal investigations, Fresenius Kabi has identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATHLETICARE Anti-Bacterial Hand Soap AC 550 (triclosan) Recalled by Petra...
The Issue: Does Not Meet Monograph: product contains, triclosan, an ingredient that can...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aspirin and Extended-release Dipyridamole Capsules Recalled by American...
The Issue: Failed Impurities/Degradation Specifications; out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxybutynin Chloride Extended-Release Tablets USP 10 mg Recalled by AVKARE...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Drospirenone and Ethinyl Estradiol Tablets Recalled by Apotex Inc. Due to...
The Issue: Contraceptive Tablets Out of Sequence: Missing or incorrect tablet placement.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thoratec HeartMate 3 Coring Tool Recalled by Thoratec Corp. Due to Small...
The Issue: Small black plastic particle was observed in the left ventricle during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...
The Issue: Temperature indicator may have changed color to dark gray or black prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...
The Issue: Temperature indicator may have changed color to dark gray or black prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...
The Issue: Temperature indicator may have changed color to dark gray or black prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx20mm-Low Profile...
The Issue: Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx30mm-Low Profile...
The Issue: Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.