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. 1,077 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
1,077 in last 12 months

Showing 16161–16180 of 53,342 recalls

DrugMay 12, 2021· American Health Packaging

Recalled Item: Sirolimus Tablets 1 mg Recalled by American Health Packaging Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
FoodMay 12, 2021· Hi Tech Pharmaceuticals

Recalled Item: Lipodrene With 25mg Ephedra Extract 100CT Recalled by Hi Tech...

The Issue: The firm was notified by the FDA that the product contains the unapproved...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 11, 2021· RC Industries Inc.

Recalled Item: Mideo's Marinara Glass 32oz jars - 6 jars per case Recalled by RC Industries...

The Issue: Potassium mg per serving on label is incorrect.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2021· DASH XCLUSIVE

Recalled Item: Imperia Elita Vitaccino Coffee Recalled by DASH XCLUSIVE Due to Marketed...

The Issue: Marketed without an approved NDA/ANDA: FDA analysis determined presence of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2021· DIBAR NUTRICIONAL S DE RL DE CV

Recalled Item: DiBAR LABS Hand Sanitizer (ethyl alcohol 70%) Recalled by DIBAR NUTRICIONAL...

The Issue: Chemical Contamination: FDA analysis found 3 lots of DiBAR hand Sanitizer to...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 11, 2021· DIBAR NUTRICIONAL S DE RL DE CV

Recalled Item: ProtectoRx (ethyl alcohol 70%) Recalled by DIBAR NUTRICIONAL S DE RL DE CV...

The Issue: CGMP Deviations: Other lots and products of hand sanitizer recalled because...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2021· DIBAR NUTRICIONAL S DE RL DE CV

Recalled Item: ADVANCE HAND SANITIZER Recalled by DIBAR NUTRICIONAL S DE RL DE CV Due to...

The Issue: CGMP Deviations: Other lots and products of hand sanitizer recalled because...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2021· DIBAR NUTRICIONAL S DE RL DE CV

Recalled Item: DiBAR LABS Hand Sanitizer Recalled by DIBAR NUTRICIONAL S DE RL DE CV Due to...

The Issue: CGMP Deviations: Other lots and products of hand sanitizer recalled because...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 11, 2021· Exactech, Inc.

Recalled Item: Humeral Augmented Tray (HAT) trials that are components of KIT-321HAT....

The Issue: The HAT trial contains a retaining ring that has shown the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Skytron, Div. The KMW Group, Inc

Recalled Item: Skyton Bracket Flatscreen Recalled by Skytron, Div. The KMW Group, Inc Due...

The Issue: Failure of the FS32 Monitor Brackets from the mounting block could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: novaplus Recalled by Medical Action Industries, Inc. 306 Due to There is a...

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· Ventec Life Systems, Inc.

Recalled Item: Ventec Life Systems VOCSN Multi-Function Ventilator Model/Version/Catalog...

The Issue: Due to a component failure, ventilators may unexpectedly shut down or have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· IMPLANTCAST GMBH

Recalled Item: EcoFit cup cementless: Model(Catalog Number)/Description: 02200046 /EcoFit...

The Issue: A risk exists during impacting of the acetabular cup into the bone the plugs...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· Randox Laboratories Ltd.

Recalled Item: NEFA CAL (Non-Esterified Fatty Acids)- IVD Standard for measurement of...

The Issue: Standard packed within NEFA kit has been assigned incorrectly. Calibrating...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· BioFire Diagnostics, LLC

Recalled Item: BioFire BCID2 Panel Recalled by BioFire Diagnostics, LLC Due to Elevated...

The Issue: Elevated rates of false negative results may occur when using blood culture...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2021· Magellan Diagnostics, Inc.

Recalled Item: LeadCare II Blood Lead Test Kit Catalog Number 70-6762 Recalled by Magellan...

The Issue: Magellan has received reports that control tests of either the Low-Control...

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

Class I — Serious Health HazardOngoing