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. 2,720 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,720 in last 12 months

Showing 36013620 of 28,744 recalls

Medical DeviceJuly 1, 2024· W L Gore & Associates, Inc.

Recalled Item: Heparin Recalled by W L Gore & Associates, Inc. Due to Due to packaging...

The Issue: Due to packaging defects, sterility assurance and heparin activity may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2024· W L Gore & Associates, Inc.

Recalled Item: Heparin Recalled by W L Gore & Associates, Inc. Due to Due to packaging...

The Issue: Due to packaging defects, sterility assurance and heparin activity may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2024· Neurovision Medical Products Inc

Recalled Item: Cobra Recalled by Neurovision Medical Products Inc Due to Mislabeling

The Issue: mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2024· Olympus Corporation of the Americas

Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...

The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2024· Olympus Corporation of the Americas

Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...

The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2024· Olympus Corporation of the Americas

Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...

The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2024· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX500 with L.x and M.x Recalled by Philips North...

The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2024· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX400 with L.x and M.x Recalled by Philips North...

The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter PST 500 U Recalled by Baxter Healthcare Corporation Due to Baxter...

The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2024· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX450 with L.x and M.x Recalled by Philips North...

The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2024· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX550 with L.x and M.x Recalled by Philips North...

The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...

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

Class II — Potential Health HazardOngoing