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 15411560 of 48,215 recalls

Medical DeviceAugust 21, 2025· Abbott Point Of Care Inc.

Recalled Item: i-STAT CG4+ cartridge (white). List Number: 03P85-25. Recalled by Abbott...

The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG4+ cartridge to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2025· Folsom Metal Products, Inc.

Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...

The Issue: Labeling includes shelf life that has not been validated.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2025· Abbott Point Of Care Inc.

Recalled Item: i-STAT CG8+ cartridge. List Number: 03P88-25. 510(k) numbers: K894914...

The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2025· Folsom Metal Products, Inc.

Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...

The Issue: Labeling includes shelf life that has not been validated.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2025· Folsom Metal Products, Inc.

Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...

The Issue: Labeling includes shelf life that has not been validated.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2025· Folsom Metal Products, Inc.

Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...

The Issue: Labeling includes shelf life that has not been validated.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2025· Abbott Point Of Care Inc.

Recalled Item: i-STAT EG7+ cartridge. List Number: 03P76-25. Recalled by Abbott Point Of...

The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...

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

Class II — Potential Health HazardOngoing
FoodAugust 20, 2025· The J.M. Smucker Company

Recalled Item: Hostess Ding Dongs CHOCOLATE CAKE WITH CREAMY FILLING 2.55 oz Recalled by...

The Issue: Mold. The firm noticed an increase in customer complaints. They conducted a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 20, 2025· Northwind Pharmaceuticals LLC

Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Northwind...

The Issue: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 20, 2025· Baxter Healthcare Corporation

Recalled Item: Acetaminophen Injection 1000 mg/100 mL (10 mg/mL) Recalled by Baxter...

The Issue: Discoloration

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 20, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Carvedilol Tablets USP Recalled by The Harvard Drug Group LLC dba Major...

The Issue: CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 20, 2025· MicroSurgical Technology Inc

Recalled Item: MST ArcDUO 9mm Recalled by MicroSurgical Technology Inc Due to An ophthalmic...

The Issue: An ophthalmic knife has a suction set (not direct patient-contacting), which...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2025· Abiomed, Inc.

Recalled Item: Automated Impella Controller (AIC) with the below brands and product...

The Issue: Specific Automated Impella Controllers (AICs) that have a Pump Driver...

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

Class I — Serious Health HazardOngoing
DrugAugust 19, 2025· Medline Industries, LP

Recalled Item: READYPREP PVP Recalled by Medline Industries, LP Due to Subpotent drug

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugAugust 18, 2025· 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
DrugAugust 18, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...

The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 18, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...

The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 18, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...

The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 18, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Amneal...

The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 18, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...

The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund