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. 2,455 recalls have been distributed to Maine in the last 12 months.
Showing 16101–16120 of 27,655 recalls
Recalled Item: BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x100mm 5.0ml PLBL Gold...
The Issue: Tubes may exhibit stopper creepout/pullout, where the stopper dissociates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quick Connect 272 KG Scale used with Maxi Sky 2 Recalled by Arjohuntleigh...
The Issue: The spreader bar can detach from the scale attachment under certain conditions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q-Connect 272 KG Scale used with Maxi Sky 2 ceiling Recalled by...
The Issue: The spreader bar can detach from the scale attachment under certain conditions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore (Radiology) - Model no. 728244 Recalled by Philips...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core - Model no. 728321 Recalled by Philips Medical Systems...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 - Model no. 728231 Recalled by Philips Medical Systems...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stanbio AC power adapter for the HemoPoint H2 meter Recalled by Stanbio...
The Issue: The US prong (type A) adapter plate may crack, break, or detach and remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE isp Implantable Port With Smooth Septum and Attachable...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Flex - Model no. 728317 Recalled by Philips Medical Systems...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT - Model no. 728326 Recalled by Philips Medical Systems...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16 Slice (Air) - Model no. 728246 Recalled by Philips Medical...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IQon Spectral CT - Model no. 728332 Recalled by Philips Medical Systems...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT - Model no. 728306 Computed Tomography X-Ray system Recalled...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.