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. 2,515 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,515 in last 12 months

Showing 2604126060 of 28,744 recalls

Medical DeviceJuly 26, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: 100/120V AC Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: TCVS is taking action to update the Operators Manual with the specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2013· Atlas Spine, Inc.

Recalled Item: Atlas Spine Torque Limiting Handle 6N-m Recalled by Atlas Spine, Inc. Due to...

The Issue: The device was not appropriately set to mitigate the risk of implant...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· Roche Molecular Systems, Inc.

Recalled Item: KIT cobas 4800 HPV AMP/DET 240T / 960T US-IVD Recalled by Roche Molecular...

The Issue: During an internal investigation, a formulation error that occurred was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· HemoCue AB

Recalled Item: HemoCue¿ Hb 201 Microcuvettes Recalled by HemoCue AB Due to HemoCue AB has...

The Issue: HemoCue AB has become aware of a production related problem involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 100NX Cassettes Recalled by Advanced Sterilization Products Due to...

The Issue: The recall of the STERRAD 100NX Cassettes was initiated because Advanced...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Folate (2500 tests) Recalled by Siemens Healthcare...

The Issue: Calibration failures and/or significant negative shifts in quality control...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Folate (100 Tests) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Calibration failures and/or significant negative shifts in quality control...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Folate (500 Tests) SMN 10325366 Recalled by Siemens Healthcare...

The Issue: Calibration failures and/or significant negative shifts in quality control...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Folate (500 tests) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Calibration failures and/or significant negative shifts in quality control...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· Velocity Medical Solutions, LLC

Recalled Item: DICOM Export Format for Sum Dose with Velocity v3.0.0. A Recalled by...

The Issue: An anomaly was detected such that, under certain conditions, a summed dose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· Medtronic Navigation, Inc.

Recalled Item: Medtronic O-arm Imaging System Mobile X-ray system. Model No. BI-700-00027...

The Issue: Review of on-system electronic product labeling and Instructions for comply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2013· OrthoPediatrics Corp

Recalled Item: 3.2mm Drill Bit. This is a component within the PediLoc Recalled by...

The Issue: OrthoPediatrics has initiated a voluntary recall of Part # 01-1050-002,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2013· Gyrus Medical, Inc

Recalled Item: GYRUS ACMI Recalled by Gyrus Medical, Inc Due to On April 29, 2013 Olympus...

The Issue: On April 29, 2013 Olympus Surgical Technologies America R&D received results...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2013· Nestle HealthCare Nutrition

Recalled Item: Nestle Nutrition Recalled by Nestle HealthCare Nutrition Due to Nestle...

The Issue: Nestle HealthCare Nutrition, Inc. is initiating a recall on some of Compat...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2013· Elekta, Inc.

Recalled Item: Stereotactic Circular Collimator - 3D Line stereotatic Hardware Accessories...

The Issue: Potential for clinical errors.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· MCKESSON TECHNOLOGIES INC

Recalled Item: Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense...

The Issue: The firm issued a clinical alert after users reported an issue where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Contra-Angle Torque Driver Kit For Certain and External Connection Product...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Contra-Angle Torque Driver Kit For Certain Internal Connection Product...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Contra-Angle Torque Driver Kit Product Usage: Molded plastic tray used...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Navigator Surgical Kit Product Usage: Molded plastic tray used in Recalled...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing