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. 2,544 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,544 in last 12 months

Showing 1448114500 of 48,215 recalls

Medical DeviceSeptember 10, 2021· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls...

The Issue: VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2021· Draeger Medical, Inc.

Recalled Item: Babylog VN500 Ventilator with Installed CO2 Measurement Option-intended for...

The Issue: Software 2.51 and Lower with Installed CO2 Measurement Option, may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2021· Inpeco S.A.

Recalled Item: FlexLab (FLX) Recalled by Inpeco S.A. Due to The Firmware (FW) of the...

The Issue: The Firmware (FW) of the Automation System Interface Module to ADVIA Centaur...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2021· Draeger Medical, Inc.

Recalled Item: Evita V500 Ventilator with Installed CO2 Measurement Option-Intended for the...

The Issue: Software 2.51 and Lower with Installed CO2 Measurement Option, may result in...

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

Class II — Potential Health HazardOngoing
DrugSeptember 9, 2021· Aurobindo Pharma USA Inc.

Recalled Item: Metoprolol Tartrate Tablets USP 100 mg Recalled by Aurobindo Pharma USA Inc....

The Issue: Presence of Foreign Substance: Product complaints received for the presence...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 9, 2021· Vi-Jon, Inc.

Recalled Item: Kroger 70% Isopropyl Alcohol First Aid Antiseptic 32 FL OZ Recalled by...

The Issue: Labeling: Label Mix-Up.The recall has been initiated after receiving one...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 9, 2021· RAYSEARCH LABORATORIES AB

Recalled Item: TomoHelical and TomoDirect plans in RayStation 6 Recalled by RAYSEARCH...

The Issue: If the dynamic jaw mode is used and an optimization is continued after...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2021· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee Recalled by...

The Issue: Packaging may include screws that are not intended to be used with the 5mm...

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

Class II — Potential Health HazardOngoing
DrugSeptember 8, 2021· Akorn, Inc.

Recalled Item: TheraTears Extra (sodium carboxymethylcellulose) 0.25% Lubricant Eye Drops...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 8, 2021· Becton Dickinson Infusion Therapy Systems Inc.

Recalled Item: BD Nexiva Recalled by Becton Dickinson Infusion Therapy Systems Inc. Due to...

The Issue: There is a breach in the product packaging that renders the product non-sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2021· Fujifilm Irvine Scientific, Inc.

Recalled Item: Vit Kit-Freeze is intended for use in assisted reproductive procedures...

The Issue: Due to a component in kit being labeled with the incorrect Expiration Date

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2021· Fujifilm Irvine Scientific, Inc.

Recalled Item: Vit Kit-Freeze is intended for use in assisted reproductive procedures...

The Issue: Due to a component in kit being labeled with the incorrect Expiration Date

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2021· Datascope Corp.

Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...

The Issue: The Helium Indicator on the Cardiosave display may over represent the amount...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2021· Datascope Corp.

Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...

The Issue: The Helium Indicator on the Cardiosave display may over represent the amount...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2021· Datascope Corp.

Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...

The Issue: The Cardiosave IABP may unexpectedly shut down when the device is running on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2021· Datascope Corp.

Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...

The Issue: The Cardiosave IABP may unexpectedly shut down when the device is running on...

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

Class II — Potential Health HazardOngoing
FoodSeptember 7, 2021· De Wafelbakkers, LLC

Recalled Item: De Wafelbakkers 18 ct Buttermilk Pancakes NET WT 1 lb. Recalled by De...

The Issue: Potential to contain Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 7, 2021· NOX MEDICAL

Recalled Item: Nox T3s Recorder - Product Usage: intended for ambulatory recording Recalled...

The Issue: Error in the device firmware results in the inaccurate detection of device...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2021· DJO, LLC

Recalled Item: Ultra-Myossage Lotion 1-gallon bottle Recalled by DJO, LLC Due to Ultrasound...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 7, 2021· DJO, LLC

Recalled Item: GEL CONDUCTOR Recalled by DJO, LLC Due to Ultrasound gels and lotions...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing