Product Recalls in Wisconsin

Product recalls affecting Wisconsin — including food, drugs, consumer products, medical devices, and vehicles distributed to Wisconsin. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,776 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
1,776 in last 12 months

Showing 5078150800 of 52,482 recalls

Medical DeviceAugust 7, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Prolactin Assay: ADVIA Centaur Calibrator B Catalog Number....

The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...

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

Class III — Low RiskOngoing
Medical DeviceAugust 7, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur FSH Assay: ADVIA Centaur Calibrator B US: Calibrator Recalled...

The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...

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

Class III — Low RiskOngoing
Medical DeviceAugust 7, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare conducted...

The Issue: GE Healthcare conducted a recall on various mobile x-ray units (Optima...

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

Class II — Potential Health HazardOngoing
DrugAugust 7, 2012· Mylan Pharmaceuticals Inc.

Recalled Item: Doxazosin Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Cross...

The Issue: Cross Contamination w/Other Products: During stability testing...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 6, 2012· Orthofix, Inc

Recalled Item: Orthofix ISKD Limb Lengthener. ISKD - Intramedullary Skeletal Kinetic...

The Issue: There is a possibility that the ISKD limb lengthener may stop distracting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...

The Issue: Although the reported incidence is low, there is the potential for the drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· ThyssenKrupp Access Corp

Recalled Item: ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically...

The Issue: The seat could break as a result of damage resulting from a seat belt being...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Elekta, Inc.

Recalled Item: Precise Digital Accelerator Delivery of radiation to defined target volumes...

The Issue: There have been a small number of instances in hospitals where the joint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Invacare Corporation

Recalled Item: Invacare¿ I-Fit" Shower Chair (Models 9780 Recalled by Invacare Corporation...

The Issue: On August 6, 2012, Invacare voluntarily recalled the Invacare¿ I-Fit" Shower...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Howmedica Osteonics Recalled by Stryker Howmedica Osteonics Corp....

The Issue: During the manufacturing of the affected lot a manufacturing error has led...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...

The Issue: Although the reported incidence is low, there is the potential for the drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Diamedix Corporation

Recalled Item: The Is-anti-Sm test kits****Catalog No: 720-240*** Product Usage: The...

The Issue: Diamedix Corporation recalled their Is-anti-Sm Test Kit due to the Positive...

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

Class II — Potential Health HazardOngoing
FoodAugust 6, 2012· Menno Beachy

Recalled Item: Menno Beachy Recalled by Menno Beachy Due to Potential Salmonella Contamination

The Issue: Salmonella Montevideo was isolated in one lot of the grape tomatoes

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 5, 2012· Reichel Foods, Inc

Recalled Item: Apple Slices & Fat Free Caramel Dip contained in the Recalled by Reichel...

The Issue: Reichel Foods is recalling these products because the sliced apples have the...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 5, 2012· Reichel Foods, Inc

Recalled Item: Dippin' Stix Sliced Apples & Caramel with Peanuts Recalled by Reichel Foods,...

The Issue: Reichel Foods is recalling these products because the sliced apples have the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 3, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Brivo XR385 DR-F/ X-Ray System X-Ray System Recalled by GE...

The Issue: GE Healthcare has become aware of a software issue on the interface of the...

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

Class II — Potential Health HazardOngoing
DrugAugust 3, 2012· Hospira Inc.

Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: A single visible particulate was observed...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 3, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: The Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: The patient support may move in an unintended manner if the foot switch...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2012· Medical Specialties Distributors, Inc.

Recalled Item: Medstream 81" (206 cm) 20 Drop Standard bore Universal Administration...

The Issue: Devices leaking at the Y-site

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2012· Covidien LLC

Recalled Item: HALO Flex Energy Generators Manufactured by B¿RRX Medical (now Covidien)...

The Issue: Potential failure of HALO Energy Generator to enter "stand by" mode when...

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

Class II — Potential Health HazardOngoing