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. 2,673 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,673 in last 12 months

Showing 1336113380 of 53,342 recalls

DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: TESTOSTERONE CYPIONATE/ DHEA *GS* 200/10MG/ML Injectable Recalled by Drug...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: TESTOSTERONE CYPIONATE/PROPIONATE *SES* Oil (10 ML) 160MG/20MG/ML Injectable...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Lansoprazole Delayed-Release Capsules Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed Dissolution Specifications; during long term stability testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: TESTOSTERONE CYPIONATE *GS* (2 mL) 80 MG/ML Injectable Recalled by Drug...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: TESTOSTERONE CYPIONATE *GS* Oil 200 MG/ML Injectable Recalled by Drug Depot,...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Lansoprazole Delayed-Release Capsules Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed Dissolution Specifications; during long term stability testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: TESTOSTERONE CYPIONATE/ANASTROZOLE *GS* OIL 200MG/1MG/ML Injectable Recalled...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: (CA) GONADORELIN (4ML) 0.2 MG/ML INJECTABLE Recalled by Drug Depot, Inc.,...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 23, 2022· Suntree Snack Foods, LLC

Recalled Item: Good & Gather Dried Sweetened Strawberries. Net Wt 4 oz Recalled by Suntree...

The Issue: Product contains undeclared Sulfites.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 23, 2022· Medtronic Vascular, Inc.

Recalled Item: Medtronic IN.PACT AV Recalled by Medtronic Vascular, Inc. Due to Packaging...

The Issue: Packaging for Balloon Catheters may be damaged resulting in loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2022· Medtronic Vascular, Inc.

Recalled Item: Medtronic IN.PACT Admiral Recalled by Medtronic Vascular, Inc. Due to...

The Issue: Packaging for Balloon Catheters may be damaged resulting in loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2022· Sight Sciences, Inc.

Recalled Item: TearCare version 1.0 SmartHubs Recalled by Sight Sciences, Inc. Due to...

The Issue: Ophthalmic devices distributed prior to the recently-obtained 510(k)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· Steris Corporation

Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 5 Recalled by Steris...

The Issue: Product not approved for release for US distribution

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· Steris Corporation

Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 2 Recalled by Steris...

The Issue: Product not approved for release for US distribution

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· American Contract Systems, Inc.

Recalled Item: ACS Cath Lab Pack Recalled by American Contract Systems, Inc. Due to Product...

The Issue: Product was sterilized with a higher than specification EO concentration.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· American Contract Systems, Inc.

Recalled Item: ACS Lap Chole Pack Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was sterilized with a higher than specification EO concentration.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· American Contract Systems, Inc.

Recalled Item: 1) ACS Spine Pack 2) ACS Lumbar/Back Set Up Tray Recalled by American...

The Issue: Product was sterilized with a higher than specification EO concentration.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· American Contract Systems, Inc.

Recalled Item: 1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack Recalled by American...

The Issue: Product was sterilized with a higher than specification EO concentration.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· American Contract Systems, Inc.

Recalled Item: ACS IR - Angio Pack Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was sterilized with a higher than specification EO concentration.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· Microbiologics Inc

Recalled Item: Inactivated macrolide-resistant Mycoplasma genitalium Recalled by...

The Issue: The QC process was not adequate for the specification range.

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

Class II — Potential Health HazardOngoing