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. 2,692 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,692 in last 12 months

Showing 1150111520 of 53,342 recalls

Medical DeviceSeptember 28, 2022· Biokit, S.A.

Recalled Item: biokitHSV-2 Rapid Test Recalled by Biokit, S.A. Due to HSV-2 rapid test may...

The Issue: HSV-2 rapid test may report false positive results.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Kamiya Biomedical Company, LLC

Recalled Item: K-ASSAY IgA Immunoturbidimetric Assay Recalled by Kamiya Biomedical Company,...

The Issue: IgA Reagent may start showing cloudiness over time, which can affect assay...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Covidien, LP

Recalled Item: Endo Stitch V-Loc 180 Absorbable Reload Recalled by Covidien, LP Due to...

The Issue: Medtronic has received 210 reports of needles breaking during endoscopic...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Covidien, LP

Recalled Item: Endo Stitch V-Loc PBT Non-Absorbable Reload Recalled by Covidien, LP Due to...

The Issue: Medtronic has received 210 reports of needles breaking during endoscopic...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health GEL PACK REUSABLE Recalled by Cardinal Health 200, LLC Due...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Reusable Gel Pack Recalled by Cardinal Health 200, LLC Due...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· X-NAV Technologies, LLC

Recalled Item: X-Guide X-Mark Probe Tool -used for registering edentulous patients to...

The Issue: Product missing one of two welds connecting the tip to the shaft, if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health GEL PACK REUSABLE Recalled by Cardinal Health 200, LLC Due...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health HOT AND COLD GEL PACK REUSABLE Recalled by Cardinal Health...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· iRhythm Technologies, Inc.

Recalled Item: Zio AT Clinical Manual Recalled by iRhythm Technologies, Inc. Due to...

The Issue: Ambulatory ECG monitoring system labeling update: 1) Clinically actionable...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2022· Synthes (USA) Products LLC

Recalled Item: SPEED 9X10X10mm Continuous Compression Implant Recalled by Synthes (USA)...

The Issue: The subject products are being recalled because they contain the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2022· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes Hammertoe Continuous Compression Implants Recalled by Synthes...

The Issue: The subject products are being recalled because they contain the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2022· Synthes (USA) Products LLC

Recalled Item: SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kit Recalled by Synthes (USA)...

The Issue: The subject products are being recalled because they contain the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2022· Synthes (USA) Products LLC

Recalled Item: SPEED 15X12X12mm Continuous Compression Implant Recalled by Synthes (USA)...

The Issue: The subject products are being recalled because they contain the incorrect...

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

Class II — Potential Health HazardOngoing
DrugSeptember 26, 2022· AuroMedics Pharma LLC

Recalled Item: Acyclovir Sodium Injection Recalled by AuroMedics Pharma LLC Due to Presence...

The Issue: Presence of Particulate Matter: Customer complaint for a dark red, brown and...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2022· AuroMedics Pharma LLC

Recalled Item: Tranexamic Acid Injection Recalled by AuroMedics Pharma LLC Due to Presence...

The Issue: Presence of Particulate Matter: Piece of metal found in a vial

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

Class III — Low RiskOngoing
Refund