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 14421–14440 of 27,655 recalls
Recalled Item: Endoform Dermal Template 2x2 Recalled by AROA BIOSURGERY Due to Potential...
The Issue: Potential for pouch seal failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoform Dermal Template 4x5 Recalled by AROA BIOSURGERY Due to Potential...
The Issue: Potential for pouch seal failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...
The Issue: The power load floor plates which hold the ambulance cot anchors in place...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical Confirm Rx Insertable Cardiac Monitor Recalled by Abbott...
The Issue: The device is unable to pair with the mobile app due to the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrex Suture Anchor Recalled by Arthrex, Inc. Due to Potentially lead to...
The Issue: Potentially lead to anchor breakage during insertion,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HeartWare Ventricular Assist HVAD System Battery Charger Model...
The Issue: HVAD Battery Charger units manufactured with wrong inductors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyberonics VNS Therapy AspireSR Recalled by LivaNova USA Inc Due to This...
The Issue: This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyberonics VNS Therapy AspireHC Model 105 Generator Recalled by LivaNova USA...
The Issue: This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LivaNova VNS Therapy System Recalled by LivaNova USA Inc Due to Lead...
The Issue: Lead impedance values reported by the affected VNS generator will be higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare 9805 and 9805P Hydraulic Patient Lifts Recalled by Invacare...
The Issue: Invacare has identified via customer complaints, the potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revanesse Versa Recalled by Prollenium Medical Technologies Inc. Due to...
The Issue: Labeling error. The product is labeled with an 18 month expiration date,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various GE Magnetic Resonance System on-site software version Product Usage:...
The Issue: Possible incorrect software version loaded.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroSet XT Injectable HA Bone Cement Recalled by Howmedica Osteonics Corp....
The Issue: Incorrect expiry date of 17-Dec-19 Correct expiry date is 11-Aug-19
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroSet XT Injectable HA Bone Cement Recalled by Howmedica Osteonics Corp....
The Issue: Incorrect expiry date of 9-Feb-20 Correct expiry date is 30-Aug-19
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Emprint Standard Percutaneous Antenna with Thermosphere Technology...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Emprint Long Percutaneous Antenna with Thermosphere Technology...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Emprint Short Percutaneous Antenna with Thermosphere Technology...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow CVC 2 Lumen Recalled by Arrow International Inc Due to The lidstock...
The Issue: The lidstock states the incorrect priming volume and flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Staclot LA 20 () The Staclot¿ LA and Staclot¿ Recalled by Diagnostica Stago,...
The Issue: There have been reports of shortened (T1-T2) results, where some instances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Staclot¿ LA () The Staclot¿ LA and Staclot¿ LA Recalled by Diagnostica...
The Issue: There have been reports of shortened (T1-T2) results, where some instances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.