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. 1,035 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
1,035 in last 12 months

Showing 22341–22360 of 53,342 recalls

DrugJuly 11, 2019· US Pharmaceuticals Inc.

Recalled Item: Wonder Freeze Pain Releiving Gel with ILEX Recalled by US Pharmaceuticals...

The Issue: CGMP Deviations: Out of Specification results for either total microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2019· US Pharmaceuticals Inc.

Recalled Item: Adult Glycerin Suppositories Recalled by US Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: Out of Specification results for either total microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2019· US Pharmaceuticals Inc.

Recalled Item: Adult Glycerin Suppositories Recalled by US Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: Out of Specification results for either total microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2019· US Pharmaceuticals Inc.

Recalled Item: Adult Glycerin Suppositories Recalled by US Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: Out of Specification results for either total microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2019· Tris Pharma Inc.

Recalled Item: Hydrocodone Polistirex and Chlorpheniramine Polistirex Extended-Release...

The Issue: Superpotent Drug and Failed Stability Specifications: High...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2019· US Pharmaceuticals Inc.

Recalled Item: Hydrocortisone Cream With Aloe Recalled by US Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations: Out of Specification results for either total microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2019· US Pharmaceuticals Inc.

Recalled Item: Eczema Lotion Hydrocortisone 1% / Anti-Itch Lotion Recalled by US...

The Issue: CGMP Deviations: Out of Specification results for either total microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 10, 2019· LNK International, Inc.

Recalled Item: Equate Night-time Sleep Aide (Diphenhydramine HCl) Recalled by LNK...

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
Medical DeviceJuly 10, 2019· Radiometer America Inc

Recalled Item: ABL90 FLEX Analyzer UDI:05700693930909 Recalled by Radiometer America Inc...

The Issue: Software Security; The action is being initiated because of software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: There is a potential for low discordant progesterone results on a subset of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 1000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: There is a potential for low discordant progesterone results on a subset of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Phadia Ab

Recalled Item: Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is Recalled by...

The Issue: code 7-102 Liquid Sensor Error

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing
DrugJuly 9, 2019· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Drospirenone and Ethinyl Estradiol Tablets Recalled by Jubilant Cadista...

The Issue: Failed dissolution specifications : failed results at the 3-month stability...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR The Simply Real Bar: Chocolate Coconut Recalled by Probar LLC Due to...

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Wholeberry Blast Recalled by Probar LLC Due to Undeclared Milk

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· FoodScience Corporation

Recalled Item: DaVinci Laboratories of Vermont Omega 3-1 Recalled by FoodScience...

The Issue: Dietary supplement mislabeled, undeclared allergen.

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

Class II — Potential Health HazardOngoing
Refund