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. 2,647 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,647 in last 12 months

Showing 1650116520 of 53,342 recalls

FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE SMORES DIETARY SUPPLEMENT NET WT. 2lb Recalled...

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE ORANGE CREAMSICLE DIETARY SUPPLEMENT NET WT....

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE CINNAMON GRAHAM CRACKER DIETARY SUPPLEMENT...

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE VANILLA ICE CREAM DIETARY SUPPLEMENT NET WT....

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2021· Hi Tech Pharmaceuticals

Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE VANILLA MILKSHAKE DIETARY SUPPLEMENT NET WT....

The Issue: During an inspection by the FDA the firm was notified by FDA that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 2, 2021· Starwest Botanicals, Inc

Recalled Item: Starwest Botanicals Item#: 209617-34 Recalled by Starwest Botanicals, Inc...

The Issue: Presence of E. coli species

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 1, 2021· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Itraconazole Capsules Recalled by Jubilant Cadista Pharmaceuticals, Inc. Due...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 1, 2021· CLINICAL LASERTHERMIA SYSTEMS AB

Recalled Item: Tranberg MR Stylet Recalled by CLINICAL LASERTHERMIA SYSTEMS AB Due to...

The Issue: single use devices labeled as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2021· CLINICAL LASERTHERMIA SYSTEMS AB

Recalled Item: Tranberg MR Cannula Recalled by CLINICAL LASERTHERMIA SYSTEMS AB Due to...

The Issue: single use devices labeled as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2021· CLINICAL LASERTHERMIA SYSTEMS AB

Recalled Item: Tranberg Laser Applicator Non-cooled Recalled by CLINICAL LASERTHERMIA...

The Issue: single use devices labeled as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2021· Stryker Leibinger GmbH & Co. KG

Recalled Item: DirectInject consists of a sterile dual paste system which is Recalled by...

The Issue: Inability for the user to inject the paste from the syringe into the target...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2021· Merits Holdings Co. dba Merits Health Products, Inc.

Recalled Item: Power Wheelchair Recalled by Merits Holdings Co. dba Merits Health Products,...

The Issue: Seat baseplate pin has broken in the field.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2021· Merits Holdings Co. dba Merits Health Products, Inc.

Recalled Item: Scooter Recalled by Merits Holdings Co. dba Merits Health Products, Inc. Due...

The Issue: Seat baseplate pin has broken in the field.

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

Class II — Potential Health HazardOngoing
DrugMarch 31, 2021· QMart

Recalled Item: IMPERIAL GOLD 2000 Recalled by QMart Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· QMart

Recalled Item: PremierZen Extreme 3000 Recalled by QMart Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· QMart

Recalled Item: Imperial Platinum 2000 Recalled by QMart Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· QMart

Recalled Item: Burro en Primavera Recalled by QMart Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Riomet (metformin hydrochloride oral solution) 500 mg/5 mL Cherry Flavor...

The Issue: Microbial Contamination of Non-Sterile Product

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· Apotex Corp.

Recalled Item: Guanfacine Extended-Release Tablets 2 mg Recalled by Apotex Corp. Due to...

The Issue: Cross Contamination with Other Product: Product is being recalled due to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 31, 2021· Soft Computer Consultants, Inc.

Recalled Item: SoftCytogenetics Recalled by Soft Computer Consultants, Inc. Due to Software...

The Issue: Software is given wrong results going out to HIS on test that had reruns.

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

Class II — Potential Health HazardOngoing