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. 2,742 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,742 in last 12 months

Showing 921940 of 53,342 recalls

Medical DeviceOctober 29, 2025· Medtronic, Inc.

Recalled Item: Aurora EV-ICD and Clinical EV-ICD Recalled by Medtronic, Inc. Due to There...

The Issue: There is a potential for delayed time to high-voltage (HV) therapy should a...

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

Class II — Potential Health HazardOngoing
DrugOctober 28, 2025· Agebox

Recalled Item: Agebox iKids-Growth (Night Formula) Recalled by Agebox Due to Undeclared...

The Issue: Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2025· Agebox

Recalled Item: Agebox iKids-Growth (Day Formula) capsules Recalled by Agebox Due to...

The Issue: Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: An out of specification results observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: An out of specification results observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: An out of specification results observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: An out of specification results observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: An out of specification results observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: An out of specification results observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: An out of specification results observed...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 28, 2025· Baxter Healthcare Corporation

Recalled Item: Welch Allyn INF BAG Recalled by Baxter Healthcare Corporation Due to...

The Issue: Replacement bladder kit for the Welch Allyn two-piece reusable blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2025· Illumina, Inc.

Recalled Item: Reagent Kits/ containing flow cells Recalled by Illumina, Inc. Due to An...

The Issue: An instrument intended for sequencing DNA libraries with in vitro diagnostic...

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

Class II — Potential Health HazardOngoing
FoodOctober 27, 2025· Pacific International Marketing

Recalled Item: Carton Label: PACIFIC FRESH VEGETABLES PACIFIC INTERNATIONAL MARKETING...

The Issue: Potential contamination with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 27, 2025· Pacific International Marketing

Recalled Item: Carton Label: PACIFIC STRAIGHT FROM THE FIELDS FRESH HERBS 4/24 Recalled by...

The Issue: Potential contamination with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 27, 2025· Pacific International Marketing

Recalled Item: Carton Label: PACIFIC FRESH VEGETABLES PACIFIC INTERNATIONAL MARKETING...

The Issue: Potential contamination with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 27, 2025· Pacific International Marketing

Recalled Item: Carton Label: PACIFIC FRESH VEGETABLES PACIFIC INTERNATIONAL MARKETING...

The Issue: Potential contamination with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 27, 2025· Otsuka ICU Medical LLC

Recalled Item: 0.9% SODIUM CHLORIDE Injection Recalled by Otsuka ICU Medical LLC Due to...

The Issue: Lack of Assurance of Sterility: Potential for flexible container leaks.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 27, 2025· Medline Industries, LP

Recalled Item: MEDLINE PERFUSION SYRINGE Recalled by Medline Industries, LP Due to Medline...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2025· Nipro Medical Corporation

Recalled Item: Hemodialysis System Recalled by Nipro Medical Corporation Due to Screw may...

The Issue: Screw may loosen or fallout of Hemodialysis system

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Fetal Monitor Model/Catalog Number: F2...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing