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. 2,563 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,563 in last 12 months

Showing 2506125080 of 53,342 recalls

Medical DeviceOctober 9, 2018· Synaptive Medical Inc

Recalled Item: BrightMatter Guide Recalled by Synaptive Medical Inc Due to This recall has...

The Issue: This recall has been initiated due to a software defect found in the Guide...

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

Class I — Serious Health HazardOngoing
DrugOctober 8, 2018· Akorn, Inc.

Recalled Item: Gentamicin Sulfate Ophthalmic Solution Recalled by Akorn, Inc. Due to...

The Issue: Presence of Particulate Matter: Crystalline particles were noticed at the 24...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 8, 2018· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility; bags have the potential to leak

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 8, 2018· ICU Medical Inc

Recalled Item: 5% Dextrose Injection Recalled by ICU Medical Inc Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; bags have the potential to leak

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 8, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS¿ Chemistry Products dLDL Reagent-GENs 26 & 27. In Vitro Recalled by...

The Issue: VITROS Chemistry Products dLDL Reagent GENs 26 and 27, negatively biased results

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: The Spirit Plus Bed Recalled by Stryker Medical Division of Stryker...

The Issue: The beds with the high rail side rail option may not be complaint with IEC...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2018· bioMerieux, Inc.

Recalled Item: bioM¿rieux NucliSENS easyMAG Lysis Buffer ref. 280134 Recalled by...

The Issue: Some eluates become colored because of remaining hemoglobin in the eluate.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: The Spirit Select Bed Recalled by Stryker Medical Division of Stryker...

The Issue: The beds with the high rail side rail option may not be complaint with IEC...

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

Class II — Potential Health HazardOngoing
DrugOctober 5, 2018· LUPIN SOMERSET

Recalled Item: Fluocinolone Acetonide Topical Solution Recalled by LUPIN SOMERSET Due to...

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

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2018· Amerigen Pharmaceuticals Inc.

Recalled Item: Temozolomide capsules Recalled by Amerigen Pharmaceuticals Inc. Due to...

The Issue: Failed dissolution specifications: Out-of-Specification dissolution results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 5, 2018· Ohmeda Medical

Recalled Item: Giraffe Omnibed - Product Usage: The OmniBed is a combination Recalled by...

The Issue: GE Healthcare has become aware of a potential safety issue that can occur if...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2018· ICU Medical, Inc.

Recalled Item: Iced Thermoset Closed-Loop Injectate Delivery System for cold Injectate. 1...

The Issue: Potential for leakage due to defect in the thermoset check valve component.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2018· ICU Medical, Inc.

Recalled Item: Thermoset Room Temperature Closed Loop Injectate Delivery System. 1 unit...

The Issue: Potential for leakage due to defect in the thermoset check valve component.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2018· ICU Medical, Inc.

Recalled Item: Iced Thermoset Closed-Loop Injectate Delivery System for cold Injectate. 1...

The Issue: Potential for leakage due to defect in the thermoset check valve component.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2018· Tosoh Bioscience Inc

Recalled Item: Hemoglobin A1c Control Recalled by Tosoh Bioscience Inc Due to Tosoh...

The Issue: Tosoh Bioscience has become aware of potential degradation of HbA1c control...

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

Class III — Low RiskOngoing
Medical DeviceOctober 5, 2018· GE Healthcare, LLC

Recalled Item: GE HEALTHCARE CARESCAPE R860 Inspiratory Safety Guard Recalled by GE...

The Issue: The ventilator Inspiratory Safety Guard (ISG) may disconnect from the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 5, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-900 Automated Immunoassay Analyzer Recalled by Tosoh Bioscience Inc Due...

The Issue: Tosoh Bioscience has become aware of a potential issue with the axis base of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2018· Covidien LLC

Recalled Item: Parietex Composite Parastomal Mesh (Product Number PCOPM15 / PCOPM20)...

The Issue: The firm is issuing this voluntary removal following receipt of reports of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-900 Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience...

The Issue: Tosoh Bioscience has become aware of a potential issue with the pickup arm...

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

Class II — Potential Health HazardOngoing
FoodOctober 4, 2018· Callie's Charleston Biscuits

Recalled Item: Callie's Charleston Biscuits COUTRY HAM BISCUITS Recalled by Callie's...

The Issue: The firm was notified by one of their vendors that the ham used in their...

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

Class I — Serious Health HazardOngoing
Refund