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. 2,708 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,708 in last 12 months

Showing 53815400 of 28,744 recalls

Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial access kit (without Prep solutions) Bit and Guard-For...

The Issue: Defect in the outer packaging of the Cranial Access Kits can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· CardioQuip, LLC

Recalled Item: CardioQuip Modular Cooler-Heater Recalled by CardioQuip, LLC Due to There is...

The Issue: There is a potential for the heating-chamber to malfunction resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit-For access to the subarachnoid space or Recalled...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit -For access to the subarachnoid space Recalled by...

The Issue: Defect in the outer packaging of the Cranial Access Kits can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra¿ Cranial Access Kit-For access to the subarachnoid space or Recalled...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· AURIS HEALTH INC

Recalled Item: Monarch Platform 100-240V- 50/60Hz 1440w Recalled by AURIS HEALTH INC Due to...

The Issue: Their is the potential that software issues may result in flipped image of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· AURIS HEALTH INC

Recalled Item: Monarch Platform Recalled by AURIS HEALTH INC Due to Their is the potential...

The Issue: Their is the potential that software issues may result in flipped image of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· AURIS HEALTH INC

Recalled Item: Monarch Platform Recalled by AURIS HEALTH INC Due to Their is the potential...

The Issue: Their is the potential that software issues may result in flipped image of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· Microbiologics Inc

Recalled Item: KWIKSTIK Recalled by Microbiologics Inc Due to A complaint investigation...

The Issue: A complaint investigation showed that the bulk pellets (lot 794-142) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· Microbiologics Inc

Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to A complaint investigation...

The Issue: A complaint investigation showed that the bulk pellets (lot 794-142) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2023· BioFire Diagnostics, LLC

Recalled Item: FilmArray TORCH . HTFA-ASY-0104 is the BIOFIRE TORCH Base Recalled by...

The Issue: Due to an increased risk of degradation of the power entry switch resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2023· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel Recalled by BioFire...

The Issue: Routine quality control testing of affected blood culture identification...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS icono (ceiling configuration) Recalled by Siemens Medical Solutions...

The Issue: Potential hardware issue for ARTIS icono ceiling system: collision sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2023· Zimmer Biomet Spine Inc.

Recalled Item: Vitality Polyaxial Screw Recalled by Zimmer Biomet Spine Inc. Due to Spinal...

The Issue: Spinal fixation system 7.5mmx 50mm screws are packaged with the correct...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Tracheostomy care kits: (1) Medline Tracheostomy Clean and Care Tray...

The Issue: The component tracheostomy brush has a sharp edge at the tip that can...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 16, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Nurse Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...

The Issue: The component tracheostomy brush has a sharp edge at the tip that can...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 16, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Nursing Skills kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: The component tracheostomy brush has a sharp edge at the tip that can...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 13, 2023· Baxter Healthcare Corporation

Recalled Item: Novum IQ Syringe infusion system Recalled by Baxter Healthcare Corporation...

The Issue: Baxter is issuing an Urgent Medical Device Correction for the Novum IQ...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 13, 2023· Breas Medical, Inc.

Recalled Item: with Notch 22M/15F sold as part of Breas Medical MPV circuit 2 pc Kits:...

The Issue: Produced with unintended open slits on the side of the mouthpiece body, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2023· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS Model Number BF-XT190 Recalled by...

The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...

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

Class I — Serious Health HazardOngoing