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. 2,371 recalls have been distributed to Maine in the last 12 months.
Showing 22001–22020 of 27,655 recalls
Recalled Item: Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number:...
The Issue: The potential exists for the Oscillating Saw Attachment to disengage from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems Recalled by...
The Issue: Medtronic is conducting a voluntary recall of all former Covidien Trellis 6...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost Release 4.0.3 Recalled by Philips Electronics North...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Lipase Reagent Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens internal investigation confirmed that current contamination...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Fem-Flex II Femoral Arterial Cannula 8 Recalled by...
The Issue: Edwards Lifesciences is recalling Fem-Flex II Pediatric Femoral Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sedecal SA Mobile Diagnost w DR x-ray system Recalled by Sedecal USA, Inc....
The Issue: Due to a software defect, the system may sporadically apply the default x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Homocysteine test system - Homocysteine Reagent. 05385415190 Recalled by...
The Issue: Customers complained about under-recovery of non-Roche controls and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carter-Thomason II Port Closure System Recalled by CooperSurgical, Inc. Due...
The Issue: The pad printing around the suture entry holes on the 15mm Suture Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...
The Issue: Deterioration in performance of the Liquid Stable (LS) 2-Part HOMOCYSTEINE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMARTABLATE RF Generator System Recalled by Biosense Webster, Inc. Due to...
The Issue: Biosense Webster is recalling the SMARTABLATE Generator System because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q/ Q zen systems Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: potential issue with the Artis Q/ Q zen systems where it is possible that an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOW PROFILE NON-LOCK SCREW Recalled by Biomet, Inc. Due to A Biomet...
The Issue: A Biomet investigation found that the Low Profile Non-Locking Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Dual Chamber Temporary External Pacemaker Recalled by Medtronic...
The Issue: Possible performance issue when used with specific AA-sized (LR6) batteries....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Monopty Disposable Core Biopsy Instruments and Kits Recalled by Bard...
The Issue: Bard Peripheral Vascular is recalling the Bard Monopty Disposable Core...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD99 Catalog number PM008 AA Recalled by Biocare Medical, LLC Due to A drop...
The Issue: A drop in staining intensity over time has been observed. These lots may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Vital Signs LightWand Stylet. A device inserted into an Recalled...
The Issue: Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nuclear Gamma Cameras (ADAC Vertex Classic Recalled by Philips Medical...
The Issue: During clinical use of a Vertex Plus Gamma Camera, as the detector heads...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Introduction Pack. A device inserted into an endotracheal tube to Recalled...
The Issue: Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to GE Healthcare has recently...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama Patient Monitoring Network Recalled by Mindray DS USA, Inc. dba...
The Issue: Software anomaly in the Panorama System software version 8.9 that manifests...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.