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. 2,622 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,622 in last 12 months

Showing 2066120680 of 53,342 recalls

DrugDecember 6, 2019· Lannett Company, Inc.

Recalled Item: Levetiracetam Oral Solution 100mg/mL Recalled by Lannett Company, Inc. Due...

The Issue: Microbial Contamination of Non-sterile Products: Out-of-specification...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 6, 2019· Gourmet International Ltd.

Recalled Item: Butler's Dark Chocolate with Irish Whisky Recalled by Gourmet International...

The Issue: undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 6, 2019· Karl Storz Endoscopy

Recalled Item: Karl Storz SE & Co. KG Recalled by Karl Storz Endoscopy Due to The firm has...

The Issue: The firm has become aware that there is a potential that the glass cover at...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2019· Medtronic Navigation, Inc.

Recalled Item: Mazor X Surgical System Positioner Type II Recalled by Medtronic Navigation,...

The Issue: There is a potential for the surgical system to detach from the operational...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2019· Stryker GmbH

Recalled Item: Stryker T2 Alpha Delta Strike Plate IMN Instruments - part Recalled by...

The Issue: Instrument can break at the level of the thread when being exposed to high...

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

Class II — Potential Health HazardOngoing
DrugDecember 4, 2019· American Health Packaging

Recalled Item: Raloxifene Hydrochloride Tablets Recalled by American Health Packaging Due...

The Issue: Failed Dissolution Specifications: Low out of specification results obtained...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 4, 2019· Werner Gourmet Meat Snacks, Inc.

Recalled Item: Jolly Rancher product is hard candies Recalled by Werner Gourmet Meat...

The Issue: Jolly Rancher product is recalled due to undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA Advance (iDXA with enCORE v16) bone densitometer Recalled by GE...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA bone densitometer Recalled by GE Healthcare, LLC Due to An issue...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v18) bone densitometer...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v17) bone densitometer...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· Johnson & Johnson Surgical Vision Inc

Recalled Item: Healon GV PRO 0.85 mL Recalled by Johnson & Johnson Surgical Vision Inc Due...

The Issue: Ophthalmic viscosurgical device may be difficult to remove from the eye,...

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

Class II — Potential Health HazardOngoing
DrugDecember 2, 2019· AuroMedics Pharma LLC

Recalled Item: Moxifloxacin Ophthalmic Solution USP Recalled by AuroMedics Pharma LLC Due...

The Issue: Discoloration: Market complaints of discoloration in Moxifloxacin Ophthalmic...

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

Class III — Low RiskOngoing
Refund
DrugDecember 2, 2019· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Amantadine Hydrochloride Tablets Recalled by Jubilant Cadista...

The Issue: Presence of Foreign Substance: Presence of a foreign object in a single tablet.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 2, 2019· 3-D Matrix, Inc.

Recalled Item: PuraSinus Absorbable Nasal Hemostat Recalled by 3-D Matrix, Inc. Due to The...

The Issue: The boxes used by the shipper were not validated for use during transport.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Argon Medical Devices, Inc

Recalled Item: BioPince Full Core Biopsy Instrument 16ga x 15cm. Recalled by Argon Medical...

The Issue: Incorrect product labeling.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: Henry Schein CardioChek Starter Kit Recalled by Polymer Technology Systems,...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: Henry Schein CardioChek Plus Professional Analyzer Recalled by Polymer...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing