Product Recalls in Minnesota
Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,693 recalls have been distributed to Minnesota in the last 12 months.
Showing 1381–1400 of 29,186 recalls
Recalled Item: C9-3io Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L11-3 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNI III TEE Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orascoptic Superior Visualization Custom loupes with Dragonfly frames...
The Issue: Due to complaints, loupe nose pads containing nickel may cause an allergic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D2TCD Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C5-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L15-7IO TRANSDUCER Transducer Probe Recalled by Philips Ultrasound, Inc Due...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X7-2t Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C9-5ec Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orascoptic Superior Visualization Custom loupes configured with Phantom...
The Issue: Due to complaints, loupe nose pads containing nickel may cause an allergic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L17-5 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C10-3v Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orascoptic Superior Visualization Phantom Essential kit ( Nose pad Recalled...
The Issue: Due to complaints, loupe nose pads containing nickel may cause an allergic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S8-3 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S12-4 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S7-2t Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3-1 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE HealthCare OEC 9800. Recalled by GE Medical Systems, LLC Due to GE...
The Issue: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE HealthCare OEC 9900 Elite C-arm Systems. Recalled by GE Medical Systems,...
The Issue: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sparrow Ascent Patient Controller Recalled by Spark Biomedical Inc Due to...
The Issue: Due to manufacturing issue, neurostimulator device may experience "cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.