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. 2,526 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,526 in last 12 months

Showing 2522125240 of 28,744 recalls

Medical DeviceDecember 16, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 50 Sterilization System Recalled by Advanced Sterilization Products...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2013· Codman & Shurtleff, Inc.

Recalled Item: CODMAN CERTAS Programmable Valves Recalled by Codman & Shurtleff, Inc. Due...

The Issue: Ensuring all customers have the tools to assist in verifying the setting of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System Recalled by Terumo...

The Issue: Sterility of medical devices intended for use in surgical procedures may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Giraffe¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Stand-Alone Resuscitation Recalled by GE Healthcare Due to Medical device...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· King Systems Corp.

Recalled Item: King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is Recalled...

The Issue: On December 13, 2012, King Systems initiated a voluntary recall of one (1)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Upgrade Kit Recalled by GE Healthcare Due to Medical device adjustment knob...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Panda iRes¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2013· AdvanDx, Inc.

Recalled Item: AdvanDx Gram-Negative QuickFISH BC. In-Vitro Diagnostic for the...

The Issue: Kits incompatible with certain fluorescence microscope light sources

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

Class III — Low RiskOngoing
Medical DeviceDecember 11, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...

The Issue: GE Healthcare has become aware of a potential safety issue involving the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2013· Toshiba American Medical Systems Inc

Recalled Item: TSX-301C Aquilion One (Vision Edition) Computed Tomography X-Ray System....

The Issue: Toshiba America Medical Systems, Inc. initiated this recall due to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2013· BioHorizons Implant Systems Inc

Recalled Item: External Implant RBT Recalled by BioHorizons Implant Systems Inc Due to The...

The Issue: The body length of the External Implant 40105D3 Lot 1302762 labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2013· Zimmer, Inc.

Recalled Item: Versys Build-Up Block The VerSys CRC Hip System is indicated Recalled by...

The Issue: Zimmer is initiating a lot specific recall of the CPT Hip Stem, Versys...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2013· Zimmer, Inc.

Recalled Item: Trabecular Metal (TM) Reverse Glenosphere 36mm Part 00-4349-036-11 The...

The Issue: Zimmer is initiating a lot specific recall of the CPT Hip Stem, Versys...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator with CO2/EtCO2 Measurement The...

The Issue: MRx defibrillator displays a -?- for EtCO2 and does not display EtCO2 values...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2013· Zimmer, Inc.

Recalled Item: CPT Hip System Recalled by Zimmer, Inc. Due to Zimmer is initiating a lot...

The Issue: Zimmer is initiating a lot specific recall of the CPT Hip Stem, Versys...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT & Brilliance iCT SP Computed Tomography X-Ray Systems...

The Issue: Patient images exhibited ring artifacts.

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

Class II — Potential Health HazardOngoing