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. 2,520 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,520 in last 12 months

Showing 2980129820 of 53,342 recalls

Medical DeviceJuly 24, 2017· Sorin Group Italia SRL - CRF

Recalled Item: Platinium DR DF4 1540 Recalled by Sorin Group Italia SRL - CRF Due to There...

The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2017· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: FUJINON ED-530XT. This device is intended for the visualization of Recalled...

The Issue: An update to the design and labeling was implemented to help reduce patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Implant Direct Swish Duo-Grip Healing Collar Recalled by Implant Direct...

The Issue: The Swish Duo-Grip Healing Collar part number 9048-13H (4.8mm) package...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2017· Howmedica Osteonics Corp.

Recalled Item: Accolade and Restoration hip product Recalled by Howmedica Osteonics Corp....

The Issue: Inner and outer sterile barriers not fully sealed.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2017· Howmedica Osteonics Corp.

Recalled Item: Accolade and Restoration hip product Recalled by Howmedica Osteonics Corp....

The Issue: Inner and outer sterile barriers not fully sealed.

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

Class II — Potential Health HazardOngoing
FoodJuly 21, 2017· Professional Complementary Health Formulas, LLC

Recalled Item: Professional Formulas Sublinqual B12 High-Potency dietary supplement...

The Issue: Sublinqual B12 tablets are recalled because the ingredients statement...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 21, 2017· Bush Brothers & Co

Recalled Item: BUSHS BEST¿ Country Style THICK Recalled by Bush Brothers & Co Due to During...

The Issue: During an FDA inspection the firm was informed that cans may have defective...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 21, 2017· GRANDE PRODUCE LTD CO

Recalled Item: Caribena yellow maradol papaya packed in 35 pound cases Recalled by GRANDE...

The Issue: Product is contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 21, 2017· Bush Brothers & Co

Recalled Item: BUSH'S BEST¿ Brown Sugar Hickory SWEET HICKORY SAUCE WITH BROWN Recalled by...

The Issue: During an FDA inspection the firm was informed that cans may have defective...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 21, 2017· Bush Brothers & Co

Recalled Item: BUSHS BEST¿ Original SEASONED WITH BACON & BROWN SUGAR BAKED Recalled by...

The Issue: During an FDA inspection the firm was informed that cans may have defective...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 21, 2017· Chiavna Saffron LLC

Recalled Item: Super Panther 7K Capsules 1250 mg blend Recalled by Chiavna Saffron LLC Due...

The Issue: Marketed without an Approved NDA/ANDA;FDA analysis found product to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 20, 2017· Beckman Coulter Inc.

Recalled Item: Sekisui Diagnostics Sekure Chemistry Acetaminophen L3K Recalled by Beckman...

The Issue: Reagent carryover from Sekisui ACTH when utilized on the BEC AU 680 analyzer...

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

Class II — Potential Health HazardOngoing
FoodJuly 20, 2017· Grandma's Herbs

Recalled Item: "Because They Work" GRANDMA'S HERBS CHOLESTEROL SUPPORT Recalled by...

The Issue: Grandmas Herbs Cholesterol has undeclared soy lecithin.

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

Class III — Low RiskOngoing
Refund
FoodJuly 19, 2017· TRULY GOOD FOODS

Recalled Item: Pumpkin Seeds Recalled by TRULY GOOD FOODS Due to Undeclared Allergen

The Issue: Undeclared allergen Tree Nuts: Blackened Seasoned Pumpkin Seeds mixed up...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2017· AVKARE Inc.

Recalled Item: Voriconazole Tablets Recalled by AVKARE Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Out of specification for a...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 19, 2017· Genicon, Inc.

Recalled Item: GENICON EZEE Retrieval Recalled by Genicon, Inc. Due to Plastic handle is...

The Issue: Plastic handle is breaking off of shaft inhibiting proper removal per...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2017· Roche Diagnostics Corporation

Recalled Item: cobas 6000 Modular Series system Recalled by Roche Diagnostics Corporation...

The Issue: A warning is being added to the cobas¿ 6000 MODULAR Series System - c501 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2017· Medline Industries Inc

Recalled Item: Sterile Elastic Esmark Bandage Recalled by Medline Industries Inc Due to...

The Issue: Product did not undergo correct sterilization procedures and may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2017· Roche Diagnostics Corporation

Recalled Item: cobas 8000 Modular Analyzer Series Recalled by Roche Diagnostics Corporation...

The Issue: A warning is being added to the cobas¿ 6000 analyzer and the cobas¿ 8000...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2017· Vyaire Medical

Recalled Item: AirLife(TM) Reduced Heparin ARTERIAL BLOOD SAMPLER Recalled by Vyaire...

The Issue: Lot #0001047501 of the 9025RHTR ABG sampling kits have been manufactured...

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

Class II — Potential Health HazardOngoing