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. 1,081 recalls have been distributed to Michigan in the last 12 months.
Showing 13201–13220 of 29,286 recalls
Recalled Item: PROX LAT HUMERAL LOCK PLATE Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various fixation systems and accessories Recalled by Zimmer Biomet, Inc. Due...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceramic Femoral Heads Recalled by Zimmer Biomet, Inc. Due to Non-highly...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various temporary devices used during the implantation of the device...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NCB PERIPROSTHETIC Recalled by Zimmer Biomet, Inc. Due to Non-highly...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity M300 telemetry monitoring device Software versions VG2.3.1 and...
The Issue: The devices have potential cybersecurity vulnerabilities, which can include...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stratum Foot Plating System-NL LP Screw 3.5x50mm ST Recalled by Nextremity...
The Issue: Product labeled as STRM-NL-3550ST, NL LP Screw 3.5x50mm ST, lot M1151 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Tourniquet Cuff 30" (Blue) Recalled by Stryker Sustainability...
The Issue: Tourniquet cuffs are potentially mislabeled. If used may lead to (1) Device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators EndoGator . Kit for Olympus 140/160/180/190 Series GI Recalled by...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators EndoGator . Kit for Olympus 140/160/180/190 Series GI Recalled by...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators Endo Smartcap Endoscope Tubing. Recalled by Medivators, Inc. Due...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators Endo Smartcap Endoscope Tubing. . Packaged as Contents 1 Recalled...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators Endo carry-on Procedure Kit - Product Usage: Recalled by...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators Endo Smartcap Endoscope Tubing. Recalled by Medivators, Inc. Due...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators Endo Smartcap Endoscope Tubing. Recalled by Medivators, Inc. Due...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas infinity central lab / cobas infinity core license-a Calculator/Data...
The Issue: Cobasinfinity laboratory solution Version 2.4.1 through Version 2.5.4 Using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EZ-IO Intraosseous Vascular Access System 25mm Needle+Stabilizer Kit...
The Issue: The safety cap attached to needles within the needle sets may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EZ-IO Intraosseous Vascular Access System 45mm Needle+Stabilizer Kit...
The Issue: The safety cap attached to needles within the needle sets may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EZ-IO Intraosseous Vascular Access System 15mm Needle+Stabilizer Kit...
The Issue: The safety cap attached to needles within the needle sets may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilite Optilite Rheumatoid Factor Kit Recalled by The Binding Site Group,...
The Issue: Assigned Rheumatoid Factor (RF) calibrator value for calibrator component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.