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 2578125800 of 28,744 recalls

Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Abbott Medical Optics, Inc.

Recalled Item: STAR ActiveTrak Excimer Laser System Recalled by Abbott Medical Optics, Inc....

The Issue: This corrective action will address an identified failure of the lamp and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2013· CooperSurgical, Inc. D.B.A. Lone Star Medical Products

Recalled Item: Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Recalled by CooperSurgical,...

The Issue: CooperSurgical is recalling two lots of 900-863 because the wrong package...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2013· Southern Implants, Inc

Recalled Item: Tri-Nex Healing Abutment Recalled by Southern Implants, Inc Due to Southern...

The Issue: Southern Implants is recalling the Tri-Nex healing abutment because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2013· Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical

Recalled Item: NX3 Try-In Gel. The product is used as a tooth shade resin material....

The Issue: Kerr Corporation is voluntarily recalling one lot of NX3 Try-In Gel, because...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2013· Mesa Laboratories, Inc.

Recalled Item: pH 7.0 Buffer Solution Pint and Quart Bottles Recalled by Mesa Laboratories,...

The Issue: Mesa Laboratories, Inc. is recalling certain lots of pH 7.0 Buffer Solution...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2013· Beckman Coulter Inc.

Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the Access 2 Immunoassay System because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2013· Maquet Medical Systems USA

Recalled Item: MAQUET Getinge Group CARDIOHELP Base Unit .7999 .8012 Recalled by Maquet...

The Issue: It has come to the attention of MAQUET that in certain rare instances, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· Leica Microsystems, Inc.

Recalled Item: Leica Ceiling Mount MSF-1 for use with M841 and M501 Recalled by Leica...

The Issue: The ceiling mount supplier encountered an event in which the drive screw in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· ArjoHuntleigh Inc.

Recalled Item: The Rotoprone therapy System is an advanced patient care system Recalled by...

The Issue: The lock pin can become stuck in the "in" position during the manual...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· SonoSite, Inc.

Recalled Item: P21x/5-1 MHz transducer Recalled by SonoSite, Inc. Due to FUJIFILM SonoSite...

The Issue: FUJIFILM SonoSite Inc. remove P21x/5-1 Transducer because the firm...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· Leica Microsystems, Inc.

Recalled Item: Leica Ceiling Mount MS-1F & MC-1F for use with the Recalled by Leica...

The Issue: The ceiling mount supplier encountered an event in which the drive screw in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: The Artis zee / zeego Angiography System is designed as Recalled by Siemens...

The Issue: There is a potential issue on running Artis systems running software VC1x...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· Harvest Technologies Corporation

Recalled Item: Harvest Graft Delivery System Recalled by Harvest Technologies Corporation...

The Issue: Potential for leur connector to leak or have cracks.

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

Class II — Potential Health HazardOngoing