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. 1,610 recalls have been distributed to Maine in the last 12 months.
Showing 3861–3880 of 27,655 recalls
Recalled Item: Medtronic Ascenda Intrathecal Catheter Recalled by Medtronic Neuromodulation...
The Issue: Design update to the Ascenda Intrathecal Catheter Models 8780, 8781, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with Eccentric Tips labeled as: 1) SOL-M 10ml Eccentric Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with Luer Slip Tips labeled as: 1) SOL-M 1ml Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringe Tip Caps labeled as: 1) SOL-M Syringe Tip Cap Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with Low Dead Space labeled as: a) SOL-M 1ml Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with exchangeable needles labeled as: SOL-CARE: 1) SOL-CARE 10ml...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Source iQ Flex M. Portable cart and platform that Recalled by First...
The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Medical SureStep Foley Tray System Recalled by C.R. Bard Inc Due to...
The Issue: Some of the devices may function incorrectly resulting in no temperature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with Fixed Needles labeled as: a) SOL-M: 1) SOL-M Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus LS-Manual Defibrillator Recalled by Remote Diagnostic...
The Issue: Simultaneous ECG measurements with multiple devices, including a manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Source Vision M. Portable cart and platform that supports Recalled by...
The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Hoffman LRF Wire Tensioner Recalled by Stryker GmbH Due to The...
The Issue: The adjustment ring on the device may become loose resulting in the wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate System Monitor Recalled by Thoratec Corp. Due to System...
The Issue: System monitor screen may display atypical behavior: Overlapping...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Range Verifier - In vitro...
The Issue: The results generated by the VITROS Immunodiagnostic Products Vitamin B12...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centrella Max - The Centrella Smart+ Bed is intended for Recalled by Baxter...
The Issue: There is a potential for the top cover of the hospital bed mattress to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient...
The Issue: Reports of patient burns.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement Battery List Number SUB0000864 Recalled by ICU Medical Inc Due...
The Issue: Due to a manufacturing defect from the battery supplier, affected batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement Battery List Number SUB0000594 and SUB0000864 found in Plum...
The Issue: Due to a manufacturing defect from the battery supplier, affected batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORI Starter Kit Recalled by Blue Belt Technologies, Inc Due to CORI...
The Issue: CORI Surgical System with Real Intelligence Software exhibits an increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN BACTISEAL EVD Catheter Set - Indicated for gaining access Recalled by...
The Issue: Defect in the external sterile packaging (pouch) leading to a gap or/and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.