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. 2,355 recalls have been distributed to Maine in the last 12 months.
Showing 26921–26940 of 27,655 recalls
Recalled Item: Terumo Advanced Perfusion System 1 System 1 Base Recalled by Terumo...
The Issue: Terumo Cardiovascular Systems has received reports of several issues that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System 8000 Base Product Usage: The Sarns Modular Perfusion System Recalled...
The Issue: During a retrospective review of complaint events, TCVS identified on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx monitor/defibrillators Models: M3535A and M3536A...
The Issue: Therapy Cable Connection wear may lead to a malfunction in detection of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx monitor/defibrillators Models: M3535A Recalled by...
The Issue: HeartStart MRx Unexpected Pads/Paddles ECG Failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Select Medical Products Vinyl Powder-Free Exam Gloves Recalled by Gulf South...
The Issue: Gulf South Medical Supply recalled their Select Medium and Large size Vinyl...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo.plaza Radiological Image Processing System Usage: Radiological...
The Issue: Firm has become aware of an unintended behavior when using syngo.plaza and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EOS X-ray Medical Diagnostic Recalled by Eos Imaging Inc Due to It was...
The Issue: It was discovered of several generator failures of the EOS System due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand Arthroscope and Hardware Set Tray (sterilization tray)...
The Issue: The gravity steam, Ethylene Oxide (EO) and STERRAD 100S sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD NX Cassette Recalled by Advanced Sterilization Products Due to...
The Issue: Advanced Sterilization Products (ASP) is recalling (removing) the Sterrad...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 100S Cassette Recalled by Advanced Sterilization Products Due to...
The Issue: Advanced Sterilization Products (ASP) is recalling (removing) the Sterrad...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion EnVe Ventilator Designed for use on patients who require Recalled...
The Issue: CareFusion identified that the EnVe Ventilator may not hold the set Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIRS for MATRIX Spine System. Minimally Invasive Reduction Screw (MIRS)...
The Issue: Synthes is initiating a Medical Device Labeling Correction following a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 9000 Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian brand Varian Eclipse Treatment Planning System for radiotherapy...
The Issue: Varian has identified an anomaly with the Eclipse Treatment Planning (for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: superDimension Systems AAS00016-xx with Software Version 4.0-4.9. Indicated...
The Issue: superDimension, Inc., is conducting a recall of certain superDimension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1. System 1 base 220/240V. The Recalled by...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Stealth 360-degree Orbital Atherectomy Device (OAD) Recalled by...
The Issue: CSI has initiated a recall on specific lot numbers of Stealth 360-degree...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.