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. 2,609 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,609 in last 12 months

Showing 2132121340 of 53,342 recalls

DrugOctober 9, 2019· Ingenus Pharmaceuticals Llc

Recalled Item: Leucovorin Calcium Injection Recalled by Ingenus Pharmaceuticals Llc Due to...

The Issue: Crystallization: Presence of particulate matter identified as API...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 9, 2019· Stryker Sustainability Solutions

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Nextremity Solutions

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Draegar Medical Systems, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2019· Roche Diagnostics Operations, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2019· Teleflex Medical

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2019· Teleflex Medical

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2019· Teleflex Medical

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.

Class II — Potential Health HazardOngoing
DrugOctober 7, 2019· Mylan Laboratories Limited (Sterile Products Division)

Recalled Item: Rifampin for Injection Recalled by Mylan Laboratories Limited (Sterile...

The Issue: Failed Impurities/Degradation Specifications: discoloration due to elevated...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 7, 2019· Nova Ortho-Med Inc

Recalled Item: Star 8 Rolling Walker/Rollator Recalled by Nova Ortho-Med Inc Due to Walkers...

The Issue: Walkers within the identified serial range have the potential for the front...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· The Binding Site Group, Ltd.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Edwards Lifesciences, LLC

Recalled Item: Oxymetry Cable Recalled by Edwards Lifesciences, LLC Due to Intermittent...

The Issue: Intermittent communication due to inconsistent crimping of connectors onto...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Implant Direct Sybron Manufacturing LLC

Recalled Item: Legacy 3 Implant Recalled by Implant Direct Sybron Manufacturing LLC Due to...

The Issue: Some dental implant packages contain incorrect implants, which could lead to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing