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. 2,463 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,463 in last 12 months

Showing 4408144100 of 53,342 recalls

Medical DeviceJune 6, 2014· Becton Dickinson & Co.

Recalled Item: CDC Anaerobe 5% Sheep Blood Agar CDC Anaerobe 5% Sheep Recalled by Becton...

The Issue: A low level of surface and subsurface contamination of Listeria...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2014· Becton Dickinson & Co.

Recalled Item: TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM) // Recalled by Becton...

The Issue: A low level of surface and subsurface contamination of Listeria...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips Medical System Allura Xper X-Ray Angiographic Recalled by Philips...

The Issue: In certain circumstances, a software error can lead to a situation where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2014· Spacelabs Healthcare Inc

Recalled Item: Spacelabs Healthcare Qube Compact Monitor Recalled by Spacelabs Healthcare...

The Issue: Spacelabs Healthcare is recalling Qube Compact Monitor, Model 91390, due to...

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

Class II — Potential Health HazardOngoing
FoodJune 6, 2014· Green Smoothie Girl

Recalled Item: GreenSmoothieGirl TriOmega Superfood Recalled by Green Smoothie Girl Due to...

The Issue: The products contain Organic Sprouted Chia Powder that may be contaminated...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 6, 2014· Hospira Inc.

Recalled Item: Heparin Sodium in 5% Dextrose Injection Recalled by Hospira Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility: Confirmed consumer report of fluid leaking...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2014· Estee Lauder Inc

Recalled Item: DENBLAN Anticavity Fluoride Toothpaste Recalled by Estee Lauder Inc Due to...

The Issue: Stability Data Does Not Support Expiry

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

Class III — Low RiskOngoing
Refund
DrugJune 5, 2014· Teva Pharmaceuticals USA

Recalled Item: Carbidopa and Levodopa Tablets USP Recalled by Teva Pharmaceuticals USA Due...

The Issue: Failed Tablet/Capsule Specifications: Teva is recalling one lot of Carbidopa...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2014· Valeant Pharmaceuticals North America LLC

Recalled Item: APLENZIN¿ (bupropion hydrobromide) Recalled by Valeant Pharmaceuticals North...

The Issue: Labeling: Incorrect or Missing Package Insert

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

Class III — Low RiskOngoing
Refund
DrugJune 5, 2014· Valeant Pharmaceuticals North America LLC

Recalled Item: APLENZIN¿ (bupropion hydrobromide) Recalled by Valeant Pharmaceuticals North...

The Issue: Labeling: Incorrect or Missing Package Insert

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

Class III — Low RiskOngoing
Refund
DrugJune 5, 2014· Valeant Pharmaceuticals North America LLC

Recalled Item: APLENZIN¿ (bupropion hydrobromide) Recalled by Valeant Pharmaceuticals North...

The Issue: Labeling: Incorrect or Missing Package Insert

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 101 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Argon Medical Devices, Inc

Recalled Item: UltraStream Exchange Kit Model Numbers 32001524 (24 cm) Recalled by Argon...

The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Argon Medical Devices, Inc

Recalled Item: UltraStream Chronic Hemodialysis Catheter Standard Kit Recalled by Argon...

The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis or Artis zee system Product Usage: Axiom Artis Recalled by...

The Issue: There is a potential problem with the AXIOM Artis or Artis zee system in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Excelsior Medical Corp

Recalled Item: Excelsior Medical Sterile Triple Lead Tubing Set and Sterile Heavy Recalled...

The Issue: There is a potential for a leak. A molding defect in the connector that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Humidifier Adaptor Recalled by Teleflex Medical Due to The seals of the...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing