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. 2,524 recalls have been distributed to Maine in the last 12 months.
Showing 7021–7040 of 27,655 recalls
Recalled Item: Monofilament Nylon Suture (McKesson Branded) and Coated Braided Silk Suture...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novafil Monofilament Polybutester Suture Product Description: 8886 4002-41...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgipro Monofilament Polypropylene Sutures Product Description CP-535...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Surgical Patties Recalled by Integra LifeSciences Corp. Due to...
The Issue: Integra LifeSciences identified that one lot was released with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lamaze Chill Teether Recalled by Tomy International Inc. Due to Affected...
The Issue: Affected lots of the product are being recalled due to potential microbial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Source Administration Set (SAS) used with the Medrad Intego PET Infusion...
The Issue: Black specks may be present on the packaged needles
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ActiveAid 922 Recalled by Altimate Medical, Inc. Due to Device manufactured...
The Issue: Device manufactured with a component with affects the foldability of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beaver EdgeAhead Stiletto/MVR Knife .90mm Straight (20G)-for ocular...
The Issue: Packaging sterile barrier has been compromised. Open seals can lead to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSS Modular Arthrodesis Nail Recalled by Biomet, Inc. Due to Product missing...
The Issue: Product missing the four small locking collar bolts resulting in extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acutrak 2 Part Number/Part Description: 30-0021 25.0mm Acutrak 2¿ - Recalled...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual-Trak Clavicle Screws Part Number/Part Description: 40-0136 3.0mm x 80mm...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AcuTwist Acutrak Compression Screws Part Number/Part Description: AI-0010-S...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Products are labeled as: Skippack Medical Lab SARS-CoV-2 Antigen Rapid...
The Issue: Distribution of SARS-CoV-2 Antigen Rapid Test Kits without FDA market...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos Agile Max (VE10 Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos dRF Max (VE10 Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMINOS Lotus Max (VF11) Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revaclear 300 dialyzers. Indicated for treatment of chronic and acute...
The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revaclear 400 dialyzers. Indicated for treatment of chronic and acute...
The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revaclear 400 Dialyzer. Product Code: 114749M. Not distributed in the...
The Issue: Potential for Internal Blood Leaks due to a twisted gasket in the dialyzer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.