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. 2,460 recalls have been distributed to Maine in the last 12 months.
Showing 15961–15980 of 48,770 recalls
Recalled Item: Implantable cardioverter defibrillators (ICD): 1) Evera family: Evera XT DR...
The Issue: A small percentage of implanted cardiac devices, from a well-defined subset,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista HDLC - colorimetric method Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....
The Issue: Failed Impurities/ Degradation Specifications - OOS for know impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....
The Issue: Failed Impurities/ Degradation Specifications - OOS for know impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....
The Issue: Failed Impurities/ Degradation Specifications - OOS for know impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enoxaparin Sodium Injection Recalled by Apotex Corp. Due to Labeling; Label...
The Issue: Labeling; Label Mixup; syringe barrels may containing markings for 150 mg/mL...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enoxaparin Sodium Injection Recalled by Apotex Corp. Due to Labeling; Label...
The Issue: Labeling; Label Mixup; syringe barrels may contain markings for 100 mg/mL...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America Llc Due to...
The Issue: Manufacturing failed to follow process steps resulting in the distribution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom Ophthalmic Surgical Procedure Packs Recalled by Alcon Research,...
The Issue: Reports have been received concerning mold found on gowns included in custom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scott¿ Moisturizing Foam Hand Sanitizer Recalled by Kimberly-Clark...
The Issue: Labeling; Label Mix-up; some bottles containing Foam Skin Cleanser soap are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Feth-R-Kath Catheter Recalled by Epimed International, Inc. Due to Outer...
The Issue: Outer coating of the catheter may deteriorate and result in the coating to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Velocity Disposable Bipolar Ablators - Product Usage: intended to be...
The Issue: There can be a potential breach of the sterile packaging barrier due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Disposable Bipolar Ablators - Product Usage: intended to be Recalled...
The Issue: There can be a potential breach of the sterile packaging barrier due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HNM Disposable Bipolar Ablators - Product Usage: intended to be used for...
The Issue: There can be a potential breach of the sterile packaging barrier due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Auryxia (ferric citrate) tablets Recalled by Akebia Therapeutics dba Keryx...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: S-Series Equipment Management System Recalled by Stryker Communications Due...
The Issue: The manufacturer has become aware that there is a likelihood that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Basic (N) 180-Drager Breathing Circuits/Anesthesia Sets Order...
The Issue: Y-piece may become detached from the ventilation hose either before or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia gas-machine - Product Usage: intended for use in administering...
The Issue: Maquet Critical Care AB received complaints where the FiCO2 value was not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Watertrap (N) 180-Drager Breathing Circuits/Anesthesia Sets Order...
The Issue: Y-piece may become detached from the ventilation hose either before or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Anesthesia (N) 180 - Drager Breathing Circuits/Anesthesia Sets...
The Issue: Y-piece may become detached from the ventilation hose either before or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.