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 25812600 of 27,833 recalls

Medical DeviceNovember 13, 2024· Alcon Research LLC

Recalled Item: Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Recalled...

The Issue: Increase in complaints associated with a molding defect within the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· Aerin Medical, Inc.

Recalled Item: Aerin Medical VivAer Stylus Recalled by Aerin Medical, Inc. Due to Some...

The Issue: Some units in a single production lot were programmed incorrectly which will...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ST REPROCESSED BRUNS CURETTE #00 (BC00) Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Magnesium Flex reagent cartridge Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics is recalling two lots of their Dimension...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ST OR MAYO HEGAR NEEDLEHOLDER 6"(OR2500) Recalled by MEDLINE INDUSTRIES, LP...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: STERILE MAGILL FORCEP (MAGF9) Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: O.R. SCISSORS Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Weak...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: RUMMELL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Weak seals...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: STERILE STRT KELLY HEMOSTAT (SK8039S) Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ST IUD REMOVAL HOOK 10" (504090) Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura Xper Systems (R7.6-R8.1). Labeled as the following: 1....

The Issue: Potential safety issues in Allura Xper R7.6- R8.1 systems where the Lifetime...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2024· Gauthier Biomedical, Inc.

Recalled Item: TriALTIS TORQUE LIMITER Recalled by Gauthier Biomedical, Inc. Due to An out...

The Issue: An out of specification component may result in the device exhibiting torque...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2024· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Presource Kits: 1) KIT Recalled by Cardinal Health 200, LLC...

The Issue: Potential for endotoxin contamination in non-sterile surgical strips and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2024· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Presource Kits: 1) KIT Recalled by Cardinal Health 200, LLC...

The Issue: Potential for endotoxin contamination in non-sterile surgical strips and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2024· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Presource Kits: 1) UROLOGY ROBOTIC PACK Recalled by Cardinal...

The Issue: Potential for endotoxin contamination in non-sterile surgical strips and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2024· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Presource Kits: 1) LARYNGOSCOPY PACK Recalled by Cardinal...

The Issue: Potential for endotoxin contamination in non-sterile surgical strips and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2024· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Presource Kits: 1) KIT Recalled by Cardinal Health 200, LLC...

The Issue: Potential for endotoxin contamination in non-sterile surgical strips and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2024· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Presource Kits: 1) KIT Recalled by Cardinal Health 200, LLC...

The Issue: Potential for endotoxin contamination in non-sterile surgical strips and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2024· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Presource Kits: 1) KIT Recalled by Cardinal Health 200, LLC...

The Issue: Potential for endotoxin contamination in non-sterile surgical strips and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2024· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Presource Kits: 1) KIT Recalled by Cardinal Health 200, LLC...

The Issue: Potential for endotoxin contamination in non-sterile surgical strips and...

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

Class II — Potential Health HazardOngoing