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 1114111160 of 48,215 recalls

Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Movable Core Wire Guide (Tefcor) Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Bentson Wire Guide Recalled by Cook Incorporated Due to Cook Medical...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Coons Interventional Wire Guide Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Movable Core Wire Guide (Tapered Tefcor) (OUS ONLY) Recalled by Cook...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Wire Guide (Nimble Floppy) Recalled by Cook Incorporated Due...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Fixed Core Wire Guide (Straight) Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Polymer Technology Systems, Inc. dba PTS Diagnostics, Inc.

Recalled Item: PTS Panels CHOL+GLU Test Strips () Recalled by Polymer Technology Systems,...

The Issue: Incorrect instructions for use were packaged into the final product.

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

Class III — Low RiskOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Wire Guide (Nimble) Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Cope Mandril Wire Guide (Nitinol) Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
DrugAugust 15, 2022· Ultra Chem Labs Corp

Recalled Item: Proton Armor Recalled by Ultra Chem Labs Corp Due to Chemical Contamination...

The Issue: Chemical Contamination and CGMP Deviations: trace amounts of methanol found...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2022· Ultra Chem Labs Corp

Recalled Item: Proton Armor Recalled by Ultra Chem Labs Corp Due to Chemical Contamination...

The Issue: Chemical Contamination and CGMP Deviations: trace amounts of methanol found...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 12, 2022· King's Hawaiian Bakery

Recalled Item: King's Hawaiian 10.5 oz. Pretzel Hamburger Buns () Recalled by King's...

The Issue: Ingredient used to manufacture pretzel products may have been contaminated...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 12, 2022· Encore Medical, LP

Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to Hip liner...

The Issue: Hip liner implant boxes may contain knee inserts and knee insert boxes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· Encore Medical, LP

Recalled Item: EMPOWER 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to Hip...

The Issue: Hip liner implant boxes may contain knee inserts and knee insert boxes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· Olympus Corporation of the Americas

Recalled Item: Olympus POWERSEAL 5MM Recalled by Olympus Corporation of the Americas Due to...

The Issue: An out of specification component preventing the blue retention ring from...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· Olympus Corporation of the Americas

Recalled Item: Olympus POWERSEAL 5MM Recalled by Olympus Corporation of the Americas Due to...

The Issue: An out of specification component preventing the blue retention ring from...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· Olympus Corporation of the Americas

Recalled Item: Olympus POWERSEAL 5MM Recalled by Olympus Corporation of the Americas Due to...

The Issue: An out of specification component preventing the blue retention ring from...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· DeRoyal Industries Inc

Recalled Item: DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear...

The Issue: Procedure packs contained a recalled product.

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

Class II — Potential Health HazardOngoing
FoodAugust 11, 2022· Supherb Farms

Recalled Item: IQF Fresh Frozen Dill shipped in 35 lb. cases in bulk. Supherb Farms Turlock...

The Issue: RTE Frozen Dill is being recalled after a customer tested product and...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 11, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 and IMMULITE 2000 XPi Thyroid Stimulating Immunoglobulins...

The Issue: An average negative bias of -23% with IMMULITE 2000/IMMULITE 2000 XPi...

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

Class II — Potential Health HazardOngoing