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. 2,614 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,614 in last 12 months

Showing 21212140 of 27,833 recalls

Medical DeviceFebruary 11, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) ACOUSTIC NEUROMA PACK-LF Recalled by...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) AV FISTULA PACK-LF Recalled by MEDLINE...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) LACERATION TRAY Recalled by MEDLINE...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) ANGIOGRAPHY SPECIALS Recalled by...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) C SCOPE DISPOSABLE KIT Recalled by...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) C SECTION Recalled by MEDLINE...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2025· Immuno-Mycologics, Inc

Recalled Item: Candida ID Antigen Recalled by Immuno-Mycologics, Inc Due to Candida...

The Issue: Candida Immunodiffusion Antigen may have reduced sensitivity which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2025· Brainlab AG

Recalled Item: Origin Data Management software versions 3.1.0 Recalled by Brainlab AG Due...

The Issue: Under certain circumstances, it can occur that patient records from...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2025· Alcon Research LLC

Recalled Item: Alcon Custom Pak with Non-Latex Symbol Recalled by Alcon Research LLC Due to...

The Issue: Customer-designed sterile surgical procedure packs contain latex components...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2025· CardioFocus, Inc.

Recalled Item: CardiFocus Heartlight X3 Catheter- Intended in the treatment of atrial...

The Issue: Damage to the sterile barrier pouch of catheter, which could potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LABOR & DELIVERY PPS Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: DR DIULUS INJECTION PACK Recalled by American Contract Systems Inc Due to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: DIAGNOSTIC NEURO IR TRAY Recalled by American Contract Systems Inc Due to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LABOR & DELIVERY PACK Recalled by American Contract Systems Inc Due to ACS...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LAPAROSCOPY PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: DELIVERY PACK Recalled by American Contract Systems Inc Due to ACS is unable...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LACERATION TRAY Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: GENERAL ANGIO PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: C-SECTION PPS Recalled by American Contract Systems Inc Due to ACS is unable...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis: Anesthesia Station ES Recalled by CareFusion 303, Inc. Due to Sync...

The Issue: Sync timeout may occur between the server and automated dispensing device,...

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

Class II — Potential Health HazardOngoing