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. 2,645 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,645 in last 12 months

Showing 1702117040 of 53,342 recalls

Medical DeviceFebruary 1, 2021· Bovie Medical Corporation

Recalled Item: HNM Disposable Bipolar Ablators - Product Usage: intended to be used for...

The Issue: There can be a potential breach of the sterile packaging barrier due to the...

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

Class II — Potential Health HazardOngoing
DrugJanuary 29, 2021· Akebia Therapeutics dba Keryx Biopharmaceutials, Inc

Recalled Item: Auryxia (ferric citrate) tablets Recalled by Akebia Therapeutics dba Keryx...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 29, 2021· Stryker Communications

Recalled Item: S-Series Equipment Management System Recalled by Stryker Communications Due...

The Issue: The manufacturer has become aware that there is a likelihood that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2021· Draeger Medical, Inc.

Recalled Item: ID Circuit Basic (N) 180-Drager Breathing Circuits/Anesthesia Sets Order...

The Issue: Y-piece may become detached from the ventilation hose either before or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2021· Getinge Group Logistics America, LLC

Recalled Item: Anesthesia gas-machine - Product Usage: intended for use in administering...

The Issue: Maquet Critical Care AB received complaints where the FiCO2 value was not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2021· Draeger Medical, Inc.

Recalled Item: VentStar Watertrap (N) 180-Drager Breathing Circuits/Anesthesia Sets Order...

The Issue: Y-piece may become detached from the ventilation hose either before or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2021· Draeger Medical, Inc.

Recalled Item: VentStar Anesthesia (N) 180 - Drager Breathing Circuits/Anesthesia Sets...

The Issue: Y-piece may become detached from the ventilation hose either before or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2021· Draeger Medical, Inc.

Recalled Item: VentStar Basic (N) 180- Drager Breathing Circuits/Anesthesia Sets Order...

The Issue: Y-piece may become detached from the ventilation hose either before or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2021· Confirm Biosciences Inc

Recalled Item: Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma)...

The Issue: Due to two (2) issues: 1) The firm distributed COVID-19 Rapid Test Cassettes...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2021· Confirm Biosciences Inc

Recalled Item: Orient Gene COVID- 19 IgG/ IgM Rapid Test Cassette (Whole Recalled by...

The Issue: Due to two (2) issues: 1) The firm distributed COVID-19 Rapid Test Cassettes...

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

Class II — Potential Health HazardOngoing
DrugJanuary 28, 2021· Accord Healthcare, Inc.

Recalled Item: Glycopyrrolate Injection Recalled by Accord Healthcare, Inc. Due to...

The Issue: Labeling; Label Mix-up; correctly labeled 2 mL vials were packaged into...

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

Class III — Low RiskOngoing
Refund
FoodJanuary 28, 2021· Glanbia Performance Nutrition (Manufacturing), Inc

Recalled Item: think! Protein + Fiber Oatmeal Recalled by Glanbia Performance Nutrition...

The Issue: Undeclared ingredients including but not limited to pecans and almonds

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 28, 2021· Olympus Corporation of the Americas

Recalled Item: Duodenoscope and accessories Recalled by Olympus Corporation of the Americas...

The Issue: Olympus Medical Systems Corporation (OMSC) has received complaints of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2021· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit - Product Usage: Used for Continuous Renal Recalled...

The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2021· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit - Product Usage: Used for Continuous Renal Recalled...

The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2021· Baxter Healthcare Corporation

Recalled Item: Preventative Maintenance Kits G5010007) and spare part kits (G5064801 and...

The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2021· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit - Product Usage: Used for Continuous Renal Recalled...

The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...

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

Class II — Potential Health HazardOngoing
DrugJanuary 27, 2021· Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Recalled Item: Spironolactone Tablets Recalled by Bryant Ranch Prepack, Inc. dba BRP...

The Issue: Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 50 mg...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 27, 2021· Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Recalled Item: Spironolactone Tablets Recalled by Bryant Ranch Prepack, Inc. dba BRP...

The Issue: Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 27, 2021· Meitheal Pharmaceuticals Inc

Recalled Item: Cisatracurium Besylate Injection Recalled by Meitheal Pharmaceuticals Inc...

The Issue: Labeling: Label mix-up: Carton of Cisatracurium Besylate Injection, USP was...

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

Class I — Serious Health HazardOngoing
Refund