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. 2,424 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,424 in last 12 months

Showing 5046150480 of 53,342 recalls

Medical DeviceJanuary 9, 2013· GE Healthcare, LLC

Recalled Item: Ventri Discovery NM 530c Recalled by GE Healthcare, LLC Due to GE Healthcare...

The Issue: GE Healthcare has recently become aware of an incident which caused a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2013· Envoy Medical Corporation

Recalled Item: Esteem Programmer Model 6001 Recalled by Envoy Medical Corporation Due to...

The Issue: Envoy Medical is conducting a voluntary correction of a limited number of...

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

Class II — Potential Health HazardOngoing
DrugJanuary 8, 2013· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: There is the potential for solution to leak...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 8, 2013· GE Healthcare, LLC

Recalled Item: Giraffe OmniBed¿ and Giraffe Incubator p/n 6600-0723-700 (rev A and Recalled...

The Issue: Neonatal beds and incubator display boards may randomly overwrite stored...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 8, 2013· Allergen Medical

Recalled Item: SeriScaffold Surgical Scaffold Product Number: SCF10X25AGEN. Surgical mesh...

The Issue: Product is dual packaged in an inner and outer pouch, the outer pouch seal...

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

Class II — Potential Health HazardOngoing
DrugJanuary 7, 2013· West-ward Pharmaceutical Corp.

Recalled Item: Belladonna Alkaloids (hyoscyamine sulfate Recalled by West-ward...

The Issue: Presence of Foreign Substance: Uncharacteristic blacks spots were found in...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 7, 2013· Somersault Snack Co., LLC

Recalled Item: Somersault brand Cinnamon Crunch. Crunchy nuggets baked with sunflower seeds...

The Issue: During ingredient review for kosher certification, the firm discovered that...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
DrugJanuary 4, 2013· Reumofan Plus USA

Recalled Item: Reumofan Plus Recalled by Reumofan Plus USA Due to Undeclared Active

The Issue: Marketed without an approved NDA/ANDA: Product may contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 4, 2013· Actavis Pharmaceuticals

Recalled Item: buPROPion Hydrochloride Extended - Release Tablets (XL) 300 mg Recalled by...

The Issue: Failed Dissolution Specifications; 8-hours for the 18-month stability...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 4, 2013· DePuy Orthopaedics, Inc.

Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...

The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 4, 2013· DePuy Orthopaedics, Inc.

Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...

The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 4, 2013· DePuy Orthopaedics, Inc.

Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...

The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 4, 2013· DePuy Orthopaedics, Inc.

Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...

The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...

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

Class I — Serious Health HazardOngoing
DrugJanuary 3, 2013· Mobius Therapeutics LLC

Recalled Item: Mitosol (mitomycin for solution) Recalled by Mobius Therapeutics LLC Due to...

The Issue: Non-Sterility: one or more components of the kit have been found to be...

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

Class I — Serious Health HazardOngoing
Refund