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. 2,690 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,690 in last 12 months

Showing 1062110640 of 28,744 recalls

Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: RINGLOC ACETABULAR SYSTEM Self-tapping bone screws Recalled by Biomet, Inc....

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: 6.5/8.0mm Cannulated Screw System Recalled by Biomet, Inc. Due to Specific...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: Titanium IFS Recalled by Biomet, Inc. Due to Specific lots of multiple...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: RingLoc+ Quick Connect Drill Bit Recalled by Biomet, Inc. Due to Specific...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: RapidFire Clip Recalled by Biomet, Inc. Due to Specific lots of multiple...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to System...

The Issue: System does not trigger a cancel command followed by a reload of the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Tuohy-Borst Side-Arm Introducer (Shuttle Select) Recalled by Cook...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Tuohy-Borst Side-Arm Introducer (Shuttle Select) Recalled by Cook...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing