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. 2,632 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,632 in last 12 months

Showing 1848118500 of 53,342 recalls

Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Dual Collapser Recalled by Sorin Group Italia S.r.l. Due to...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 6.0 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.5 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 7.5 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 5.5 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.0 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 9.0 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 7.0 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 6.5 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayCare Recalled by RAYSEARCH LABORATORIES AB Due to When performing offline...

The Issue: When performing offline image review in RayCare 2C, RayCare 3A and RayCare...

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

Class II — Potential Health HazardOngoing
FoodJuly 28, 2020· Kader Exports Pvt. Ltd.

Recalled Item: Cooked Recalled by Kader Exports Pvt. Ltd. Due to Potential Salmonella...

The Issue: Frozen cooked shrimp is possibly contaminated with Salmonella.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 28, 2020· Medline Industries Inc

Recalled Item: Control Recalled by Medline Industries Inc Due to Product was shipped with...

The Issue: Product was shipped with (ice) instead of frozen (dry ice).

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2020· Wright Medical Technology, Inc.

Recalled Item: Screw Removal Case Assembly Recalled by Wright Medical Technology, Inc. Due...

The Issue: Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2020· Wright Medical Technology, Inc.

Recalled Item: Hardware removal kit Recalled by Wright Medical Technology, Inc. Due to...

The Issue: Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and...

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

Class II — Potential Health HazardOngoing
DrugJuly 27, 2020· Broncolin, S.A. de C.V.

Recalled Item: HERBACIL Recalled by Broncolin, S.A. de C.V. Due to Chemical Contamination:...

The Issue: Chemical Contamination: HERBACIL, Antiseptic Hand Sanitizer, 70% Alcohol,...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 27, 2020· Broncolin, S.A. de C.V.

Recalled Item: HERBACIL Recalled by Broncolin, S.A. de C.V. Due to CGMP Deviations:...

The Issue: CGMP Deviations: products were recalled because they were manufactured in...

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

Class II — Potential Health HazardOngoing
Refund