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. 2,301 recalls have been distributed to Maine in the last 12 months.
Showing 42141–42160 of 48,770 recalls
Recalled Item: Pill for weight reduction Recalled by MyNicNaxs, Inc. Due to Undeclared Active
The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SlimEasy Herbs Capsule Recalled by MyNicNaxs, Inc. Due to Undeclared Active
The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: JIANFEIJINDAN Activity Girl Capsules Recalled by MyNicNaxs, Inc. Due to...
The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Super Fat Burning Bomb Capsules Recalled by MyNicNaxs, Inc. Due to...
The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: REDUCE WEIGHT FRUTA PLANTA Capsules Recalled by MyNicNaxs, Inc. Due to...
The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magic Slim capsules Recalled by MyNicNaxs, Inc. Due to Undeclared Active
The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Slim Xtreme Weight loss capsules Recalled by MyNicNaxs, Inc. Due to...
The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Teva Hydroxyzine Pamoate Capsules Recalled by Teva Pharmaceuticals USA Due...
The Issue: CGMP Deviations: Hydroxyzine Pamoate Capsules, USP, 100 mg were manufactured...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Teva Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due...
The Issue: CGMP Deviations: Dextroamphetamine Saccharate, Amphetamine Asparate,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Teva Ethambutol Hydrochloride Tablets Recalled by Teva Pharmaceuticals USA...
The Issue: CGMP Deviations: Ethambutol Hydrochloride Tablets, USP, 400 mg were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Teva Hydroxyzine Pamoate Capsules Recalled by Teva Pharmaceuticals USA Due...
The Issue: CGMP Deviations: Hydroxyzine Pamoate Capsules, USP, 25 mg were manufactured...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Plum XL Recalled by Hospira Inc. Due to There is the potential for the door...
The Issue: There is the potential for the door roller assembly on the Plum LifeCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum XL3 Multi line Infusion System Recalled by Hospira Inc. Due to There is...
The Issue: There is the potential for the door roller assembly on the Plum LifeCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeCare 5000 Pump (Plum 1.6) infusion pump Recalled by Hospira Inc. Due to...
The Issue: There is the potential for the door roller assembly on the Plum LifeCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RetCam 3 Recalled by Clarity Medical Systems Inc Due to Software anomaly for...
The Issue: Software anomaly for RetCam 3, RetCam Shuttle and RetCam Portable with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Kodak 2100 Intraoral X-Ray System Recalled by Carestream Health Inc....
The Issue: Carestream received problem reports relating to apparent early failure of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Kodak 2200 Intraoral X-Ray System Recalled by Carestream Health Inc....
The Issue: Carestream received problem reports relating to apparent early failure of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaSure Impedance Controlled Endometrial Ablation System Radiofrequency...
The Issue: NovaSure Radiofrequency Control Units may not meet a requirement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Model: 861290 The HeartStart...
The Issue: HeartStart XL+ battery charge time to 100% capacity at 35¿C (95¿F) is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Legionella BCYE Growth Supplement Recalled by Remel Inc Due to The...
The Issue: The product may contain high levels of microbial contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.