Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,059 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,059 in last 12 months

Showing 35813600 of 27,833 recalls

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· 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 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· 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 27, 2024· Medivance Inc.

Recalled Item: Arctic Sun Temperature Management Systems Recalled by Medivance Inc. Due to...

The Issue: If temperature management system fails to reach correct target water...

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: 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· Boston Scientific Corporation

Recalled Item: Capio SLIM Suture Capturing Device Recalled by Boston Scientific Corporation...

The Issue: Some lots of Capio SLIM do not consistently catch the suture after...

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· Ventana Medical Systems, Inc.

Recalled Item: Ventana anti-CD10 (SP67) Rabbit Monoclonal Primary Antibody Recalled by...

The Issue: Their is a potential for high background and off-target staining when using...

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

Class II — Potential Health HazardOngoing