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 2658126600 of 28,744 recalls

Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: - CLEAR-TRAC COMPLETE Recalled by Surgical Instrument Service And Savings,...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: - Relieva Flex Sinus Guide Catheter (Green) Tip Shape: F-70 Recalled by...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2013· Remel Inc

Recalled Item: Streptex* kit Recalled by Remel Inc Due to The product may give weak or...

The Issue: The product may give weak or false negative test results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2013· Merit Medical Systems, Inc.

Recalled Item: Merit Medical PerfOrma Anglographic Catheter 5F Multipack Product Usage:...

The Issue: Merit Medical Systems is recalling various lots of Performa Cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2013· GE Healthcare, LLC

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

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 DeviceMay 2, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens brand MicroScan Dried Negative Breakpoint Combo 47 panels...

The Issue: The product has the potential for false negative or delayed reaction for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2013· Remel Inc

Recalled Item: Streptex* Latex D Recalled by Remel Inc Due to The product may give weak or...

The Issue: The product may give weak or false negative test results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Mobiletta Mira Mobile X-ray System Recalled by Siemens Medical Solutions...

The Issue: Siemens issued a Field Safety Alert about the potential risk to users when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· CooperSurgical, Inc.

Recalled Item: CooperSurgical TransWarmer Infant Transport Mattress with WarmGel P/N 20421...

The Issue: Trans Warmer Infant and Transport Mattress not labeled with exp.date may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· Becton Dickinson & Company

Recalled Item: BD SafetyGlide Allergy. Sterile Allergy Treatment Syringe Tray. Recalled by...

The Issue: There has been an increase in complaints regarding the needle/safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· Applied Medical Resources Corp

Recalled Item: Applied Medicals Epix¿ and Direct Drive Laparoscopic Graspers Recalled by...

The Issue: Applied Medical is conducting a voluntary recall on specific lot numbers of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· Becton Dickinson & Company

Recalled Item: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter BD Franklin Lakes...

The Issue: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter may have blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· Elekta, Inc.

Recalled Item: DMLC IV-ERGO Product Usage: Intended for use with rotating gantry Recalled...

The Issue: It is possible for an intermittent error to occur in the gantry sensor of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar Wide 670. Designed to meet the needs for lifting humans. Recalled...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar 360. Designed to meet the needs for lifting humans. Recalled by...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Nephron Pharmaceuticals Corp.

Recalled Item: EZ Breathe Medication Cup. For the delivery of liquid medications Recalled...

The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 30, 2013· American Optisurgical Inc

Recalled Item: FAST Procedure Kit. Intended for use as a Minor Surgical Procedures Tray....

The Issue: American Optisurgical, Inc initiated a recall of ChloraPrep Hi-Lite Orange...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Angiodynamics, Inc.

Recalled Item: AngioDynamics Micro Introducer Kits under the following labeling: 1)...

The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar Standard. Designed to meet the needs for lifting humans. Recalled...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar 350. Designed to meet the needs for lifting humans. Recalled by...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing