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. 2,492 recalls have been distributed to Maine in the last 12 months.
Showing 12841–12860 of 27,655 recalls
Recalled Item: Embryology Heated Plate within the RI Witness Recalled by CooperSurgical,...
The Issue: The touchpad may not work properly after cleaning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-40 plus Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-40 plus Reconditioned Instrument Recalled by Beckman...
The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-96 plus Reconditioned Instrument Recalled by Beckman...
The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-96 plus Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Recalled by Elekta Inc Due to It is possible that the...
The Issue: It is possible that the forced electron density settings will be changed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Recalled by Elekta Inc Due to It is possible that the...
The Issue: It is possible that the forced electron density settings will be changed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achilles Express Bone Sonometer Recalled by GE Healthcare, LLC Due to...
The Issue: Certain Achilles Express and Achilles Insight systems were shipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achilles Insight Bone Sonometer Recalled by GE Healthcare, LLC Due to...
The Issue: Certain Achilles Express and Achilles Insight systems were shipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Central Recalled by Spacelabs Healthcare, Inc. Due to The firm...
The Issue: The firm received reports of loss of audio alarm after a power failure or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transducer S8-3t UDI (01)00884838073524 Can be used as Recalled by Philips...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transducer S7-3t UDI (01)00884838061439 Can be used with: Recalled by...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transducer S8-3t UDI (01)00884838067523 Can be used with: Recalled by...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transducer S7-3t UDI (01)00884838067530 Used as accessory with: Recalled by...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPROTTE Lumbar with Introducer Recalled by Pajunk GmbH Due to Problem with...
The Issue: Problem with packaging sealing process which affects sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ApexPro Telemetry Server System. Also identified as Modification To: ApexPro...
The Issue: May not provide visual and/or audible alarms at the CARESCAPE Central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dario Blood Glucose Monitoring System Recalled by LABSTYLE INNOVATIONS Due...
The Issue: The Dario-Blood Glucose Tracker Android App versions 4.3.0-4.3.2 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CIRCLAMP W/1.3 CM BELL-single-use Recalled by Centurion Medical...
The Issue: A mismatch between the angle of the hole in the base and the angle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c 701 and 702 Analyzer/Module-RF interference claims for the Recalled...
The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CIRCLAMP W/1.1CM BELL - single-use Recalled by Centurion Medical...
The Issue: A mismatch between the angle of the hole in the base and the angle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.