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. 2,689 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,689 in last 12 months

Showing 1208112100 of 53,342 recalls

Medical DeviceJuly 12, 2022· FUJIFILM Healthcare Americas Corporation

Recalled Item: SCENARIA View: Software Version V1.08 Recalled by FUJIFILM Healthcare...

The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2022· FUJIFILM Healthcare Americas Corporation

Recalled Item: Surpria: Software Version V3.11 Recalled by FUJIFILM Healthcare Americas...

The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Sensis or Sensis Vibe Combo systems as follows: System Recalled by...

The Issue: The Sensis Signal Input Box provides hooks as a milled item on the bottom of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 12, 2022· Haimen Shengbang Laboratory Equipment Co. Ltd.

Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...

The Issue: Distributed VTM outside of VTM Guidance and without clearance.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2022· Haimen Shengbang Laboratory Equipment Co. Ltd.

Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...

The Issue: Distributed VTM outside of VTM Guidance and without clearance.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2022· Haimen Shengbang Laboratory Equipment Co. Ltd.

Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...

The Issue: Distributed VTM outside of VTM Guidance and without clearance.

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

Class I — Serious Health HazardOngoing
DrugJuly 11, 2022· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Tacrolimus Ointment Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Defective Container: Tube split from side seam

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

Class III — Low RiskOngoing
Refund
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Ativan Injection (lorazepam injection Recalled by Hikma Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 11, 2022· WISSNER-BOSSERHOFF GMBH

Recalled Item: SafeControl handset (a component of the Sentida bed which moves Recalled by...

The Issue: When the handset is disconnected from the power mains, and mains operation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam AXL Recalled by Oculus Optikgeraete GMBH Due to Due to a software...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam AXL Wave . Used to image the anterior segment of the eye. Recalled...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam HR . Used to image the anterior segment of the eye. Recalled by...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

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

Class II — Potential Health HazardOngoing
DrugJuly 7, 2022· Apotex Corp.

Recalled Item: Aripiprazole Tablets Recalled by Apotex Corp. Due to Failed dissolution...

The Issue: Failed dissolution specifications: OOS for dissolution at the 12-month...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 7, 2022· Olympus Corporation of the Americas

Recalled Item: ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S Recalled by Olympus...

The Issue: Mis-wired component-the improperly wired component can result in additional...

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

Class II — Potential Health HazardOngoing
FoodJuly 6, 2022· Chuckanut Bay Foods LLC

Recalled Item: Item 34033-12 Recalled by Chuckanut Bay Foods LLC Due to Undeclared Soy

The Issue: Undeclared Soy Lecithin. Label declares Chocolate Compound (Sunflower...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2022· Chuckanut Bay Foods LLC

Recalled Item: Item 34032-12 Recalled by Chuckanut Bay Foods LLC Due to Undeclared Soy

The Issue: Undeclared Soy Lecithin. Label declares Chocolate Compound (Sunflower...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2022· Chuckanut Bay Foods LLC

Recalled Item: Item 34021-12 Recalled by Chuckanut Bay Foods LLC Due to Undeclared Soy

The Issue: Undeclared Soy Lecithin. Label declares Chocolate Compound (Sunflower...

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

Class II — Potential Health HazardOngoing
Refund