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. 2,524 recalls have been distributed to Maine in the last 12 months.
Showing 8901–8920 of 27,655 recalls
Recalled Item: SOMATOM Force with software syngo.CT VB20 Model #10742326 Recalled by...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge with software syngo.CT VB20 Model #10590000 Recalled...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS with software syngo.CT VB20 Model #8098027 Recalled by...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash with software syngo.CT VB20 Model #10430603...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Confidence with software syngo.CT VB20 Model #10590100 Recalled by...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Drive with software syngo.CT VB20 Model #10431700 Recalled by...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Edge Plus with software syngo.CT VB20 Model #10267000 Recalled by...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK LOGIC Polyethylene Tibial Inserts Recalled by Exactech, Inc. Due to...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTHROFOCUS Polyethylene Tibial Inserts (Product Line: 256-12-XX Recalled by...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vantage Total Ankle System including a. Vantage Fixed-Bearing Polyethylene...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRULIANT Knee System including TRULIANT Tibial Inserts Recalled by Exactech,...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System custom devices labeled as the following:...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System Recalled by Exactech, Inc. Due to Inserts...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK All-polyethylene UNI...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK Logic RBK PS Tibial...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software BeamAdjust version 2.2 Recalled by PTW NORTH AMERICA CORPORATION...
The Issue: When a measurement with a PTW detector array is performed with the software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part...
The Issue: Due to product not meeting specification for concentricity and failing to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EcoLotion Transmission Lotion Recalled by North Coast Medical Inc Due to...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norco Ultrasound Gel Recalled by North Coast Medical Inc Due to Ultrasound...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.