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. 2,636 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,636 in last 12 months

Showing 1796117980 of 53,342 recalls

Medical DeviceSeptember 29, 2020· Verathon, Inc.

Recalled Item: BladderScan Prime Plus Probe - Product Usage: intended Recalled by Verathon,...

The Issue: Due to a change in handle material and process, probe handle may crack.

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

Class II — Potential Health HazardOngoing
DrugSeptember 28, 2020· Teligent Pharma, Inc.

Recalled Item: Fluocinonide Ointment USP 0.05% Recalled by Teligent Pharma, Inc. Due to...

The Issue: Failed Impurities/Degradation - Out-of-specification results for...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 28, 2020· Hormel Foods Corporation

Recalled Item: SKIPPY Super Chunk Peanut Butter 16.3oz packaged in Recalled by Hormel Foods...

The Issue: Aflatoxin level slightly above actionable limit

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 28, 2020· LivaNova USA Inc

Recalled Item: VNS Therapy¿ AspireSR¿ Generator Recalled by LivaNova USA Inc Due to Due to...

The Issue: Due to an extra digit being inadvertently added to the serial number of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2020· Advanced Bionics, LLC

Recalled Item: AB PowerCel 170 (velvet black) Recalled by Advanced Bionics, LLC Due to...

The Issue: Mislabeling; It has been determined that some batteries were improperly...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 26, 2020· Advanced Bionics, LLC

Recalled Item: AB PowerCel 230 (velvet black) Recalled by Advanced Bionics, LLC Due to...

The Issue: Mislabeling; It has been determined that some batteries were improperly...

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

Class III — Low RiskOngoing
DrugSeptember 25, 2020· Wishgarden Herbs, Incorporated

Recalled Item: Happy Ducts Compress Recalled by Wishgarden Herbs, Incorporated Due to...

The Issue: Microbial Contamination of a Non-Sterile Product: Product tested positive...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2020· Wishgarden Herbs, Incorporated

Recalled Item: Goldenseal POWDER Recalled by Wishgarden Herbs, Incorporated Due to...

The Issue: Microbial Contamination of a Non-Sterile Product: Product tested positive...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2020· Wishgarden Herbs, Incorporated

Recalled Item: Cord Care POWDER Recalled by Wishgarden Herbs, Incorporated Due to Microbial...

The Issue: Microbial Contamination of a Non-Sterile Product: Product tested positive...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2020· VistaPharm, Inc.

Recalled Item: NYSTATIN ORAL SUSPENSION Recalled by VistaPharm, Inc. Due to Failed...

The Issue: Failed Impurties/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 25, 2020· Stryker GmbH

Recalled Item: Osteosynthesis Compression Staple EasyClip Recalled by Stryker GmbH Due to...

The Issue: The device has the potential to release nickel above the acceptable margin...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2020· Cardinal Health 200, LLC

Recalled Item: Covidien MONOJECT Standard Hypodermic Needle Recalled by Cardinal Health...

The Issue: Potential for the needle to detach from the cartridge after the bottom of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2020· Exactech, Inc.

Recalled Item: Equinoxe Platform Fracture Stem Recalled by Exactech, Inc. Due to The device...

The Issue: The device may be incorrectly laser marked as a right stem, when it should...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2020· Exactech, Inc.

Recalled Item: Equinoxe Platform Fracture Stem Recalled by Exactech, Inc. Due to The device...

The Issue: The device may be incorrectly laser marked as a right stem, when it should...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2020· Zimmer Biomet, Inc.

Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...

The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2020· Zimmer Biomet, Inc.

Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...

The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2020· Zimmer Biomet, Inc.

Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...

The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2020· Zimmer Biomet, Inc.

Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...

The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2020· Boston Scientific Corporation

Recalled Item: AMS 700 MS Pump with and without InhibiZone Recalled by Boston Scientific...

The Issue: The recalling firm has observed an increase in complaints of problems...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2020· Zimmer Biomet, Inc.

Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...

The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...

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

Class II — Potential Health HazardOngoing