Product Recalls in Michigan
Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,537 recalls have been distributed to Michigan in the last 12 months.
Showing 26901–26920 of 53,342 recalls
Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur CB Resolve Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur OB Resolve Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Skull Pin Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percepta Quad CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm...
The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Temperature Sensor Catheter 8FR Recalled by Degania Silicone, Ltd. Due...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature sensing catheter 14FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percepta CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm and...
The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Maestro 4000 Cardiac Ablation System Recalled by Boston...
The Issue: Reports of unintended continuation of radiofrequency (RF) energy delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml...
The Issue: Label was incorrect. The label states that the volume of the retrieval bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...
The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...
The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...
The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...
The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...
The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...
The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.