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. 2,532 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,532 in last 12 months

Showing 2770127720 of 53,342 recalls

DrugMarch 28, 2018· Elroselabs Inc.

Recalled Item: Molleave Recalled by Elroselabs Inc. 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
DrugMarch 28, 2018· Elroselabs Inc.

Recalled Item: Conzerol (antipoxin) H2O2 Gel Recalled by Elroselabs Inc. 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
Medical DeviceMarch 28, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...

The Issue: The dose calculation accuracy may in some situations be less than expected....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Draegar Medical Systems, Inc.

Recalled Item: Infinity Acute Care System (lACS) Monitoring Solution Recalled by Draegar...

The Issue: Software anomaly resulting in the loss of patient settings and stored...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Ace Surgical Supply Co., Inc.

Recalled Item: Double Blade Shoe F/Unigraft Knife 1.5 Thick X 9MM SKU Recalled by Ace...

The Issue: The product inside the package is incorrect. A single blade shoe was...

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

Class II — Potential Health HazardOngoing
DrugMarch 27, 2018· AuroMedics Pharma LLC

Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...

The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 27, 2018· AuroMedics Pharma LLC

Recalled Item: Levetiracetam in 0.54% Sodium Chloride Injection Recalled by AuroMedics...

The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 27, 2018· AuroMedics Pharma LLC

Recalled Item: Levetiracetam in 0.82% Sodium Chloride Injection Recalled by AuroMedics...

The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 27, 2018· AuroMedics Pharma LLC

Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...

The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 27, 2018· AuroMedics Pharma LLC

Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...

The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 27, 2018· AuroMedics Pharma LLC

Recalled Item: Linezolid Injection 600 mg per 300 mL (2 mg/mL) For Intravenous...

The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 27, 2018· AuroMedics Pharma LLC

Recalled Item: Levetiracetam in 0.75% Sodium Chloride Injection Recalled by AuroMedics...

The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 27, 2018· Lupin Pharmaceuticals Inc.

Recalled Item: Lupin Cefdinir powder for Oral Suspension USP Recalled by Lupin...

The Issue: Superpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 27, 2018· Bestco, Inc.

Recalled Item: Signature Care Calcium Chews Recalled by Bestco, Inc. Due to A packaging...

The Issue: A packaging revision and lack of revision to the corresponding packaging...

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

Class III — Low RiskOngoing
Refund