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. 2,567 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,567 in last 12 months

Showing 1106111080 of 48,215 recalls

Medical DeviceAugust 31, 2022· Micro-X Ltd.

Recalled Item: MICRO-X ROVER MOBILE X-RAY SYSTEM Recalled by Micro-X Ltd. Due to Software...

The Issue: Software calibration error with product equip with a Dose Area Product (DAP)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2022· PHONESOAP

Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains...

The Issue: Excessive ultraviolet-C radiation

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2022· SIEMENS HEALTHCARE DIAGNOSTICS INC

Recalled Item: N Antiserum to Human IgG Recalled by SIEMENS HEALTHCARE DIAGNOSTICS INC Due...

The Issue: N Antiserum to Human IgG are not meeting the current High-Dose Hook Effect...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2022· SIEMENS HEALTHCARE DIAGNOSTICS INC

Recalled Item: N Antiserum to Human IgG Recalled by SIEMENS HEALTHCARE DIAGNOSTICS INC Due...

The Issue: N Antiserum to Human IgG are not meeting the current High-Dose Hook Effect...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2022· Synthes (USA) Products LLC

Recalled Item: Hammertoe Continuous Compression Implant (CCI) Kit Part Number: 46.239.001...

The Issue: Drill Pin (drill bit) is not compatible with the Drill Template included in...

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

Class II — Potential Health HazardOngoing
DrugAugust 29, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Inc Due to...

The Issue: Labeling: Label Error on Declared Strength; A sealed 100-count bottle...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 29, 2022· TELEFLEX LLC

Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...

The Issue: Incidents of device splitting or detaching during use

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 29, 2022· TELEFLEX LLC

Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...

The Issue: Incidents of device splitting or detaching during use

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 29, 2022· TELEFLEX LLC

Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...

The Issue: Incidents of device splitting or detaching during use

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 29, 2022· TELEFLEX LLC

Recalled Item: Filter + Catheter Mount Recalled by TELEFLEX LLC Due to Incidents of device...

The Issue: Incidents of device splitting or detaching during use

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 29, 2022· TELEFLEX LLC

Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...

The Issue: Incidents of device splitting or detaching during use

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 29, 2022· TELEFLEX LLC

Recalled Item: Iso-Gard Filter S with Expandi-Flex/Elbow: a) Recalled by TELEFLEX LLC Due...

The Issue: Incidents of device splitting or detaching during use

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 29, 2022· Ossur Americas

Recalled Item: OSSUR Power Knee OSSUR Power Knee Recalled by Ossur Americas Due to Battery...

The Issue: Battery may dislodge from the Power Knee

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

Class II — Potential Health HazardOngoing
DrugAugust 26, 2022· Carolina Infusion

Recalled Item: TRI-MIX 30/2/40 Injectable Recalled by Carolina Infusion Due to Lack of...

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
DrugAugust 26, 2022· Carolina Infusion

Recalled Item: TRI-MIX 30/1/20 Injectable Recalled by Carolina Infusion Due to Lack of...

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
DrugAugust 26, 2022· Carolina Infusion

Recalled Item: MIC/B12/L-Carn (HD) 35/35/35/1/35 MG/ML Injectable Recalled by Carolina...

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
DrugAugust 26, 2022· Carolina Infusion

Recalled Item: TEST CYP/DHEA (Sesame) 200 MG/2.5 MG/ML Injectable Recalled by Carolina...

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
DrugAugust 26, 2022· Carolina Infusion

Recalled Item: QUAD-MIX 30/2/60/0.15 Injectable Recalled by Carolina Infusion Due to Lack...

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
DrugAugust 26, 2022· Carolina Infusion

Recalled Item: Semaglutide/Cyanocobalamin 24/2 MG/ML Injectable Recalled by Carolina...

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
DrugAugust 26, 2022· Carolina Infusion

Recalled Item: TEST CYP (Grapeseed) 200 MG/ML Injectable Recalled by Carolina Infusion Due...

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