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. 2,520 recalls have been distributed to Michigan in the last 12 months.
Showing 32241–32260 of 53,342 recalls
Recalled Item: Por fullct fem st 20x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental vss bowed 19x190mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 16mmdx50cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 16mmdx48cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Por fullct fem st 16x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 14mmdx48cm right Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial IM Nail 15mmdx44cm Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYFRECATOR 2000 HANDPIECE SHEATH Recalled by ConMed Corporation Due to For...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Stryker Visum¿ LED Surgical Lighting system is intended to Recalled by...
The Issue: The potential hazard that can arise for the combination of the missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meijer Caesar Salad labeled as Meijer Greek Salad Recalled by Meijer Inc Due...
The Issue: Meijer announced it is recalling a recent shipment of its pre-made Caesar...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fusia Asian Aspirations Szechuan Stir Fry Recalled by Versa Marketing Due to...
The Issue: Product was tested and found positive for Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Liebel-Flarsheim Direct Digital Imaging System (DDIS) Liebel-Flarsheim...
The Issue: Software issue. The difference between the display and dosimeter readings In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim...
The Issue: Software issue. The difference between the display and dosimeter readings In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTECH ROSA Spine 1.0.2 The device is intended for the Recalled by Zimmer...
The Issue: Unapproved change made by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.