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. 2,531 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,531 in last 12 months

Showing 2298123000 of 28,744 recalls

Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT (Uninterruptible Power Supply (UPS) accessory devices)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF Ready (Uninterruptible Power Supply (UPS) accessory devices)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 (Uninterruptible Power Supply (UPS) accessory devices)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 64 channel with Essence Recalled by Philips Medical Systems...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Nidek Inc

Recalled Item: YC-1800 OPHTHALMIC YAG LASER SYSTEM Recalled by Nidek Inc Due to Dear Doctor...

The Issue: Dear Doctor letter and Quick Guide is being sent to users of the YC-1800 to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity TF (Uninterruptible Power Supply (UPS) accessory devices) Computed...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: CardioMD III (Uninterruptible Power Supply (UPS) accessory devices) Computed...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Diamond Select Brilliance CT 16 (Uninterruptible Power Supply (UPS)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X (Uninterruptible Power Supply (UPS) accessory devices) Computed...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte-JetStream AZ (Uninterruptible Power Supply (UPS) accessory devices)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF PET/CT 16 Slice (Uninterruptible Power Supply (UPS) accessory...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: HLS/HIT Set Advanced with Bioline and/or Softline Coating Console Product...

The Issue: A potential issue was detected that could result in blood leakage from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· Codman & Shurtleff, Inc.

Recalled Item: CODMAN 3000 Series Set- Huber needles. Used in combination Recalled by...

The Issue: Needle is leaking from hub/needle cannula connection

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Quadrox-iD Adult Diffusion Membrane Oxygenator Product Usage: The Quadrox-iD...

The Issue: A potential issue was detected that could result in blood leakage from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· GE Healthcare

Recalled Item: GE Healthcare Millennium VG Recalled by GE Healthcare Due to GE Healthcare...

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

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· SpineFrontier, Inc.

Recalled Item: SpineFrontier MISquito Percutaneous Pedicle Screw System Surgical Technique...

The Issue: The PedFuse Pedicle Screw Rod Caliper included with the MISquito Pedicle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2015· Merge Healthcare, Inc.

Recalled Item: Merge LIS software. Recalled by Merge Healthcare, Inc. Due to There is a...

The Issue: There is a potential for duplicate container numbers to be created for patients.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2015· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...

The Issue: An issue with photon dose calculation for DMLC (Dynamic MLC) plans for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2015· DePuy Orthopaedics, Inc.

Recalled Item: LCS COMPLETE RPS Femoral Implants Recalled by DePuy Orthopaedics, Inc. Due...

The Issue: The LCS COMPLETE RPS Knee System has higher rates of revision in Australia...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2015· DePuy Orthopaedics, Inc.

Recalled Item: LCS COMPLETE RPS inserts Recalled by DePuy Orthopaedics, Inc. Due to The LCS...

The Issue: The LCS COMPLETE RPS Knee System has higher rates of revision in Australia...

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

Class II — Potential Health HazardOngoing