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. 1,909 recalls have been distributed to Idaho in the last 12 months.
Showing 16101–16120 of 48,215 recalls
Recalled Item: Assure COVID-19 IgG/IgM Rapid Test Device that include: 1) Pouch Recalled by...
The Issue: Due to Products being incorrect labeling "for diagnostic use" and labelled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Consist of a distal connection mechanism (either standard Terumo Ball...
The Issue: There is a potential for the stainless steel locking plates on the device's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Radiological Image Processing System - Product Usage:...
The Issue: The wrong patient information may be displayed in the viewer or PowerJacket.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automated Impella Controller (AIC) Recalled by Abiomed, Inc. Due to...
The Issue: Retrospective reporting for the release of Technical Bulletin IMP-2643 AIC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cellex qSARS-Cov-2 Antigen Rapid Test Recalled by Cellex Due to The kit does...
The Issue: The kit does not have an emergency use authorization (EUA).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyWay Walker Chassis - Product Usage: is intended for use Recalled by James...
The Issue: Due to a failure of the welds, the casters detached from the rear legs of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasonic pulsed doppler imaging system - Product Usage: intended for...
The Issue: Arietta 850 software version 4.0.0., 4.0.1, and 4.0.2 has an error in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B&G Sweet Heat Pepper Dip Recalled by B&G Sweet Heat Peppers Due to Cream...
The Issue: Cream Cheese and Sour Cream are declared, but milk is not declared on label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Buprenorphine and Naloxone Sublingual Film 2mg/0.5mg Recalled by Alvogen,...
The Issue: Subpotent drug: Out of specification for assay of naloxone and buprenorphine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Dissolution Specifications: Out-of-specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Item #140804 Recalled by Taylor Farms Northwest, LLC Due to Undeclared Soy
The Issue: Undeclared Soy Lecithin. Croissant contains Margarine (Soy Lecithin) but...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item #140952 Recalled by Taylor Farms Northwest, LLC Due to Undeclared Soy
The Issue: Undeclared Soy Lecithin. Croissant contains Margarine (Soy Lecithin) but...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item #140946 Recalled by Taylor Farms Northwest, LLC Due to Undeclared Soy
The Issue: Undeclared Soy Lecithin. Croissant contains Margarine (Soy Lecithin) but...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: IFU and Patient Manual updated to describe HVAD Controller Connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: IFU and Patient Manual updated to describe Expected Alarm Duration. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: Medtronic HeartWare HVAD System Instructions for Use (IFU) and Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Their is a potential that...
The Issue: Their is a potential that Video Processor/Illuminators may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panther Fusion Tube Tray Recalled by Hologic, Inc Due to There is a...
The Issue: There is a potential for tube trays to leak which could potentially result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CF Delivery Dev Caps Bravo x5 Recalled by Covidien Llc Due to The capsule...
The Issue: The capsule may fail to attach to the esophageal mucosa, which in turn may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRAVO PH CAPS DELIVERY DEV5-PK Recalled by Covidien Llc Due to The capsule...
The Issue: The capsule may fail to attach to the esophageal mucosa, which in turn may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.