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. 2,563 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,563 in last 12 months

Showing 2496124980 of 53,342 recalls

FoodOctober 16, 2018· Bakkavor Foods USA, Inc.

Recalled Item: Trader Joe's Tomato & Basil Hummus Dip Recalled by Bakkavor Foods USA, Inc....

The Issue: Hummus was recalled due to potential Salmonella and/or Listeria...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 16, 2018· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...

The Issue: Devices were distributed despite the Helium-fine leak test results not being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 1500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics has identified an issue with Dimension Vista...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· ASO, LLC

Recalled Item: Family Wellness First Aid Sterile Gauze Pad 3 in x 3 in Recalled by ASO, LLC...

The Issue: Potential that gauze pads may not be fully sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...

The Issue: Devices were distributed despite the Helium-fine leak test results not being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Canon Medical System, USA, INC.

Recalled Item: Radrex-i X-Ray System (DRAD-3000E) TFP-4336W (Wireless FPD) Software...

The Issue: software malfunction; It was found when a user performs radiography using...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics has identified an issue with Dimension Vista...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...

The Issue: Devices were distributed despite the Helium-fine leak test results not being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: (1) Argon Medical Devices Stopcocks Recalled by Argon Medical Devices, Inc...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: (1) Argon Medical Devices Double Female LL Adapter Recalled by Argon Medical...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Double Male LL Adapter Recalled by Argon Medical...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices AHD Luer Lock Cap Recalled by Argon Medical Devices,...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Hemostasis Valve Recalled by Argon Medical Devices,...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Carl Zeiss Meditec, Inc.

Recalled Item: The PLEX Elite 9000 Recalled by Carl Zeiss Meditec, Inc. Due to Under...

The Issue: Under certain fault conditions, the existing design may expose the operator...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Septishield II Recalled by Argon Medical Devices, Inc...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Plugs Recalled by Argon Medical Devices, Inc Due to...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: (1) Argon Medical Devices Vascuclamp Recalled by Argon Medical Devices, Inc...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices TRI-JECT Recalled by Argon Medical Devices, Inc Due to...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
FoodOctober 15, 2018· Request Foods Incorporated

Recalled Item: Love The Wild Hawaiian Style Tropical Bowl with Barramundi 9oz. Recalled by...

The Issue: The firm was notified by their supplier that ingredients used in their...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 15, 2018· Diamond Crystal Brands, Inc.

Recalled Item: HOUSE BLEND Barbecue SAUCE INGREDIENTS: ***Contains 2% or less of Recalled...

The Issue: During a label check the firm noticed that the product was shipped with the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund