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 26812700 of 27,833 recalls

Medical DeviceOctober 28, 2024· Boston Scientific Corporation

Recalled Item: AMS Artificial Urinary Sphincter Pressure Regulating Balloon 61-70 cm H2O...

The Issue: Potential for mislabeled packaging in which a device labeled as a Pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· GE Medical Systems, LLC

Recalled Item: SIGNA Architect AIR Recalled by GE Medical Systems, LLC Due to Gradient...

The Issue: Gradient coils for certain MR systems (see affected product list in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· GE Medical Systems, LLC

Recalled Item: Discovery MR750w 3.0T Recalled by GE Medical Systems, LLC Due to Gradient...

The Issue: Gradient coils for certain MR systems (see affected product list in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· GE Medical Systems, LLC

Recalled Item: SIGNA Architect Recalled by GE Medical Systems, LLC Due to Gradient coils...

The Issue: Gradient coils for certain MR systems (see affected product list in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· GE Medical Systems, LLC

Recalled Item: Tomographic Imager Combining Emission Computed Tomography With Nuclear...

The Issue: Gradient coils for certain MR systems (see affected product list in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a...

The Issue: Due to incorrect labels applied to devices during servicing. Labels contain...

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

Class III — Low RiskOngoing
Medical DeviceOctober 25, 2024· Noah Medical

Recalled Item: Galaxy System (GAL-001) Recalled by Noah Medical Due to Bronchoscopic system...

The Issue: Bronchoscopic system uninterruptable power may have defective component, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2024· Noah Medical

Recalled Item: Galaxy bronchoscope (Product GALB-001) used with Instructions for use...

The Issue: Not all biopsy tools meant to fit bronchoscope channel (2.1mm inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ENDO KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Identified...

The Issue: Identified lots of Olympus product may be missing sterile and manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2024· GE Healthcare (China) Co., Ltd.

Recalled Item: GE Proteus XR/A radiographic system Recalled by GE Healthcare (China) Co.,...

The Issue: Steel cables in the Wall Stand for certain Proteus XR/a systems serviced by...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· Micro-X Ltd.

Recalled Item: MICRO-X Rover Mobile X-ray System Recalled by Micro-X Ltd. Due to During...

The Issue: During internal testing it was found that if the system is Ready to expose...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Lab Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Specimen...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: URINE COLLECTION VHC Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Clean Catch Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: URINE KIT W/BD CUP Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: UA KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Specimen...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: URINE COLLECTION KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: URINE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Specimen...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: URINALYSIS KIT 4 Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2024· ICU Medical, Inc.

Recalled Item: Allegedly counterfeit batteries manufactured by CSB batteries being used...

The Issue: ICU Medical has received reports of allegedly counterfeit CSB batteries...

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

Class I — Serious Health HazardOngoing