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. 2,441 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,441 in last 12 months

Showing 4558145600 of 53,342 recalls

FoodFebruary 20, 2014· Walong Marketing, Inc.

Recalled Item: Asian Taste (Brand) Green Tea Pumpkin Seeds Recalled by Walong Marketing,...

The Issue: Walong Marketing, Inc. initiated the recall of Asian Taste Green Tea Pumpkin...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 20, 2014· Laboratories Cop Inc

Recalled Item: Ideal Protein Double Chocolate Brownie. Individually wrapped Recalled by...

The Issue: Possible contamination with thin metal fragments.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 20, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS TT4 Calibrator For the quantitative measurement of total thyroxine...

The Issue: Total T4 Calibrators and Reagent Packs may have calibration failures or low...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2014· Biosense Webster, Inc.

Recalled Item: PENTARAY NAV High-Density Mapping Catheter and PENTARAY NAV ECO Catheter...

The Issue: Biosense Webster is recalling the PentaRay Nav Catheter because it has the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 19, 2014· Gilead Sciences, Inc.

Recalled Item: Atripla (efavirenz 600 mg/ emtricitabine 200 mg/ tenofovir disoproxil...

The Issue: Presence of Foreign Substance: Red Silicone Rubber Particulates are Present...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 19, 2014· Fannie May Confection Brands Inc

Recalled Item: 4 oz. Heart - Shaped Box of Assorted Chocolates Recalled by Fannie May...

The Issue: Undeclared Allergen - peanut

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 19, 2014· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Blood Glucose Monitors System. For in vitro diagnostic use...

The Issue: Abbott Diabetes Care has identified through internal testing and...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 19, 2014· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Flash Blood Glucose Monitors System. Meter made in China Recalled...

The Issue: Abbott Diabetes Care has identified through internal testing and...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 19, 2014· Medefil Incorporated

Recalled Item: Heparin I.V. Flush Syringe is available is pre-filled polypropylene syringes...

The Issue: The bar code that is printed on the Master Carton label does not correspond...

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

Class III — Low RiskOngoing
FoodFebruary 18, 2014· Newman'S Own Inc.

Recalled Item: Newman's Own Salsa Con Queso Recalled by Newman'S Own Inc. Due to Undeclared...

The Issue: Undeclared wheat

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 18, 2014· Siemens Healthcare Diagnostics

Recalled Item: ADVIA Centaur XP Immunoassay system Recalled by Siemens Healthcare...

The Issue: Instrument Cover Gas Spring failures. Over time, the gas spring may lose its...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2014· Hospira Inc.

Recalled Item: GemStar Docking Station Recalled by Hospira Inc. Due to There are two...

The Issue: There are two situations that may occur when using the GemStar Docking...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 18, 2014· Remel Inc

Recalled Item: Oxoid Vancomycin 30 mcg Recalled by Remel Inc Due to Some of the discs may...

The Issue: Some of the discs may not be impregnated with the antibiotic.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A with...

The Issue: When the HeartStart MRx.is used with the Q-CPR Meter in defibrillation mode,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Model numbers: M3535A Recalled...

The Issue: MRx may display a Red X in the Ready For Use (RFU) indicator during...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2014· Philips Medical Systems, Inc.

Recalled Item: M3536A HeartStart MRx with Wireless Link Upgrade (861289) The HeartStart...

The Issue: Wireless Link may be unable to transmit data when configured for a specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2014· Philips Medical Systems, Inc.

Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical Systems,...

The Issue: A component of the MRx Processor Board may be susceptible to damage from...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2014· Philips Medical Systems, Inc.

Recalled Item: HeartStart MRx Defibrillator/Monitor M3538A Lithium Ion Batteries Revision J...

The Issue: Philips HeartStart MRx Monitor/Defibrillator, when operating on battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical...

The Issue: ECG trunk cable and connector block of the MRx could be susceptible to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2014· Elekta, Inc.

Recalled Item: XiO RPT System The XiO RTP System is used to Recalled by Elekta, Inc. Due to...

The Issue: Dose and Monitor Unit values are not computed correctly when Elekta...

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

Class II — Potential Health HazardOngoing