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. 2,594 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,594 in last 12 months

Showing 48614880 of 48,215 recalls

Medical DeviceJuly 25, 2024· Breas Medical, Inc.

Recalled Item: Vivo 45 LS Recalled by Breas Medical, Inc. Due to There is a potential for...

The Issue: There is a potential for short term (<7 days) elevated levels of...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 25, 2024· Intrinsic Therapeutics, Inc.

Recalled Item: Barricaid Annular Closure Impactor Recalled by Intrinsic Therapeutics, Inc....

The Issue: At least two units have been found to be missing a weld.

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

Class II — Potential Health HazardOngoing
DrugJuly 24, 2024· B. Braun Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B. Braun Medical Inc Due to...

The Issue: Presence of Particulate Matter

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 24, 2024· Cardinal Health 200, LLC

Recalled Item: (a) CardinalHealth Salem Sump Dual Lumen Stomach Tube with Anti- Valve...

The Issue: The firm received reports of breakage in the Anti- Valve (ARV) due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· TMJ Solutions Inc

Recalled Item: Stryker TMJ Unilateral Implant Recalled by TMJ Solutions Inc Due to...

The Issue: Patient-fitted temporomandibular (TMJ) prothesis contained incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Cardinal Health 200, LLC

Recalled Item: (a) CardinalHealth Salem Sump Dual Lumen Stomach Tube Recalled by Cardinal...

The Issue: The firm received reports of breakage in the Anti- Valve (ARV) due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· ROi CPS LLC

Recalled Item: regard Clinical Packaging Solutions Recalled by ROi CPS LLC Due to Medical...

The Issue: Medical convenience kits were distributed with Merit syringes (manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Coarse Diamond Round Recalled by Stryker Corporation Due...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 2.0mm Diamond Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 5.0mm Coarse Diamond Round Recalled by Stryker Corporation Due...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Diamond Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Cypress Medical Products LLC

Recalled Item: McKesson Syringe 60CC Recalled by Cypress Medical Products LLC Due to...

The Issue: Affected syringes lack FDA clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Precision Match Head Recalled by Stryker Corporation Due...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 4.0mm Coarse Diamond Round Recalled by Stryker Corporation Due...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 4.0mm Diamond Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 4.0mm Precision Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Precision Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Diamond Match Head Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

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

Class II — Potential Health HazardOngoing
DrugJuly 23, 2024· FDC Limited

Recalled Item: Ciprofloxacin ophthalmic solution USP Recalled by FDC Limited Due to...

The Issue: Defective container: unable to get the solution out of the bottle as the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

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

Class II — Potential Health HazardOngoing