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. 2,507 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,507 in last 12 months

Showing 3568135700 of 53,342 recalls

Medical DeviceMay 12, 2016· Baxter Healthcare Corp

Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...

The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...

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

Class II — Potential Health HazardOngoing
DrugMay 11, 2016· The Aloe Source

Recalled Item: aloe SPORT liniment TOPICAL ANALGESIC 8 fl oz. tube Recalled by The Aloe...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2016· Profarma Distributors LLC

Recalled Item: 1% Clotrimazol cream Recalled by Profarma Distributors LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2016· Profarma Distributors LLC

Recalled Item: VERMOX Tablets 500 mg Recalled by Profarma Distributors LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2016· Profarma Distributors LLC

Recalled Item: tabcin ACTIVE M.R. Capsules Recalled by Profarma Distributors LLC Due to...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2016· Profarma Distributors LLC

Recalled Item: VERMOX Tablets 100 mg Recalled by Profarma Distributors LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2016· Profarma Distributors LLC

Recalled Item: tabcin NOCHE Recalled by Profarma Distributors LLC Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 11, 2016· Whole Foods Market

Recalled Item: Whole Foods Market Korean BBQ Sauce NET WT 12 OZ Recalled by Whole Foods...

The Issue: Undeclared peanut and coconut.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 11, 2016· Siemens Healthcare Diagnostics Inc.

Recalled Item: Hettich Centrifuge Modules: StreamLAB Centrifuge Module (10372372 or...

The Issue: Premature bucket failures

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2016· Synthes (USA) Products LLC

Recalled Item: Norian Drillable Inject 10 CC-Sterile Recalled by Synthes (USA) Products LLC...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2016· Zimmer Biomet, Inc.

Recalled Item: Persona Trabecular Metal Tibia Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Zimmer Inc. is initiating a recall of specific Persona" Trabecular Metal"...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2016· Synthes (USA) Products LLC

Recalled Item: Norian Drillable Inject 3 CC-Sterile Recalled by Synthes (USA) Products LLC...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2016· Synthes (USA) Products LLC

Recalled Item: Norian Drillable Inject 5 CC-Sterile Recalled by Synthes (USA) Products LLC...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...

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

Class II — Potential Health HazardOngoing
DrugMay 10, 2016· Allergan Sales, LLC

Recalled Item: Tazorac (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...

The Issue: Failed Content Uniformity Specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 10, 2016· Allergan Sales, LLC

Recalled Item: Tazorac (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...

The Issue: Failed Content Uniformity Specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 10, 2016· Bayer Health Care LLC

Recalled Item: Coppertone SUNSCREEN LOTION Recalled by Bayer Health Care LLC Due to...

The Issue: Labeling; Product Contains Undeclared API (Oxybenzone)

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 10, 2016· Frontier Natural Products CO-OP

Recalled Item: 16 oz. foil packages of Frontier Co-op Hojicha Tea Certified Recalled by...

The Issue: Product potentially contaminated with Salmonella.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 10, 2016· Karlsburger Foods, Inc.

Recalled Item: Karlsburger Recalled by Karlsburger Foods, Inc. Due to Undeclared Allergen

The Issue: Karlsburger Foods Inc., is recalling 2 lb containers of Mesquite Seasoning...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 10, 2016· Medical Vision Ab

Recalled Item: Double Pump RF Patient Cassette Recalled by Medical Vision Ab Due to...

The Issue: Sterility of device may be compromised due to sterile package breakage.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2016· CarboFix Orthopedics, Ltd.

Recalled Item: Piccolo Composite Tibia and Femoral Nailing Systems - Ball Tip Recalled by...

The Issue: Firm received complaints where the Piccolo Composite Ball Tip Guide Wire...

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

Class II — Potential Health HazardOngoing