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. 2,558 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,558 in last 12 months

Showing 1968119700 of 28,744 recalls

Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: CARDIAC KIT WITH 03 ml FLUSH DEVICE Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: ICN TRANSDUCER KIT W/30ML FLUSH DEVICE FOR STANFORD UNIV. HOSP. Recalled by...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: PERFUSION KIT FOR UNIV. OF IOWA Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: CATH LAB KIT w/4 PORT "ON" MANIFOLD Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: QUAD KIT WITH THREE TRANSPAC¿ AND 03ML FLUSH DEVICES FOR ST. FRANCIS HOSP....

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: Transpac¿ IV Monitoring Kit w/Safeset 84" Arterial Pressure Tubing Recalled...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: TRANSPAC¿ IV MONITORING KIT Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: ARTERIAL SET-UP W/03ML FLUSH DEVICE FOR ORLANDO REG. MED. CTR. Recalled by...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: OPEN HEART KIT W/03ML FLUSH DEVICE FOR CUMBERLAND COUNTY HOSP. Recalled by...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: Cath Lab Kit w/Waste Bag System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: Transpac¿ IV Monitoring Kit Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: TRANSPAC¿ IV MONITORING KIT WITH SAFESET" RESERVOIR AND BLOOD SAMPLING PORT...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: Cath Lab Kit w/03 ml Intraflo Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2016· Hamilton Medical, Inc.

Recalled Item: Hamilton-MR1 Ventilator: Catalog# 161010 The Hamilton MR1 Ventilator is...

The Issue: Oxygen tubing and the oxygen connector of the Hamilton-MR1 could potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2016· Cardinal Health 200, LLC

Recalled Item: V. Mueller Neuro/Spine Recalled by Cardinal Health 200, LLC Due to Potential...

The Issue: Potential risk associated with corrosion demonstrated on the distraction...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2016· Merit Medical Systems, Inc.

Recalled Item: Manifold Kit. Catalog Number K09-11867AP Recalled by Merit Medical Systems,...

The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2016· GE OEC Medical Systems, Inc

Recalled Item: OEC Brivo 715 Prime Recalled by GE OEC Medical Systems, Inc Due to GE...

The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC Brivo...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2016· Merit Medical Systems, Inc.

Recalled Item: Procedure Kit. Catalog Numbers K12-04830B and K12-YP030A Recalled by Merit...

The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2016· Merit Medical Systems, Inc.

Recalled Item: Fluid Management Set. Catalog Number K08-MP5159A Recalled by Merit Medical...

The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2016· Merit Medical Systems, Inc.

Recalled Item: Waste Management Kit. Catalog Number K10-04381AP Recalled by Merit Medical...

The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...

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

Class II — Potential Health HazardOngoing