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. 983 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
983 in last 12 months

Showing 26921–26940 of 48,215 recalls

FoodDecember 7, 2017· Ventura Foods, LLC

Recalled Item: Smokehouse 220 Sweet & Spicy Barbecue Sauce Recalled by Ventura Foods, LLC...

The Issue: A plastic foreign object was inadvertently introduced into the product...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 7, 2017· Ventura Foods, LLC

Recalled Item: A&W All American Food Papa Sauce Recalled by Ventura Foods, LLC Due to...

The Issue: A plastic foreign object was inadvertently introduced into the product...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 7, 2017· Ventura Foods, LLC

Recalled Item: Classic Gourmet Dressing Recalled by Ventura Foods, LLC Due to Foreign...

The Issue: A plastic foreign object was inadvertently introduced into the product...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 7, 2017· Ventura Foods, LLC

Recalled Item: Sysco Imperial Tartar Sauce Recalled by Ventura Foods, LLC Due to Foreign...

The Issue: A plastic foreign object was inadvertently introduced into the product...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 7, 2017· Ventura Foods, LLC

Recalled Item: Sysco Imperial Glazed Hot Bacon Dressing Recalled by Ventura Foods, LLC Due...

The Issue: A plastic foreign object was inadvertently introduced into the product...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2017· SCA Pharmaceuticals

Recalled Item: Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride 10 mL in Single Dose...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date - product label was...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2017· Johnson & Johnson

Recalled Item: Neutrogena deep clean purifying whipped foam cleanser Recalled by Johnson &...

The Issue: Defective Container: products showed leakage (bubbles, foaming) of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2017· Johnson & Johnson

Recalled Item: Neutrogena Elevated 4-Holiday Trays (contains Neutrogena Deep Clean...

The Issue: Defective Container: products showed leakage (bubbles, foaming) of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2017· BotanicalNow

Recalled Item: BodySlim Herbal Advanced technology & Strong formula capsules Recalled by...

The Issue: Marketed without an approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 7, 2017· Johnson & Johnson

Recalled Item: Neutrogena Acne Proofing whipped foam cleanser Recalled by Johnson & Johnson...

The Issue: Defective Container: products showed leakage (bubbles, foaming) of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 6, 2017· Reliance Medical Products Inc

Recalled Item: Suspension Arm (P/N: 525004 Recalled by Reliance Medical Products Inc Due to...

The Issue: Product has been found with a missing Washer, Retaining Ring, and/or Stop...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2017· Intel-GE Care Innovations LLC

Recalled Item: Health Harmony Mobile application software Product Usage: Care Innovations...

The Issue: It was discovered that in certain situations, including partial sessions and...

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

Class II — Potential Health HazardOngoing
DrugDecember 5, 2017· Sanofi-Aventis U.S. LLC

Recalled Item: Enoxaparin Sodium Recalled by Sanofi-Aventis U.S. LLC Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength. A single syringe labeled as 150...

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

Class III — Low RiskOngoing
Refund
FoodDecember 5, 2017· Creative Contract Packaging Corporation, LLC

Recalled Item: HERB-OX Beef Flavor Granulated Bouillon Recalled by Creative Contract...

The Issue: Creative Contract Packaging LLC is voluntarily recalling two code dates of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 4, 2017· Cellavision AB

Recalled Item: CellaVision DM Software versions 6.0.1 or 6.0.2 installed on the Recalled by...

The Issue: A software malfunction was found where WBC, RBC and PLT comments added after...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Accord Media, LLC

Recalled Item: Truth Renew Plus Recalled by Accord Media, LLC Due to Distribution of...

The Issue: Distribution of medical devices with unapproved green LED light used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Smiths Medical ASD Inc.

Recalled Item: PORT-A-CATH II PS/Titan Recalled by Smiths Medical ASD Inc. Due to Certain...

The Issue: Certain models and lots of PORT A CATH implantable port kits may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Beckman Coulter Inc.

Recalled Item: iChem VELOCITY Urine Chemistry Strips Recalled by Beckman Coulter Inc. Due...

The Issue: A subset of Lot 7212154 A of the iChem VELOCITY Urine Chemistry strips has...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Accord Media, LLC

Recalled Item: Ultra Renew Recalled by Accord Media, LLC Due to Distribution of medical...

The Issue: Distribution of medical devices with unapproved green LED light used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Accord Media, LLC

Recalled Item: Truth Renew Recalled by Accord Media, LLC Due to Distribution of medical...

The Issue: Distribution of medical devices with unapproved green LED light used to...

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

Class II — Potential Health HazardOngoing