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. 1,073 recalls have been distributed to Idaho in the last 12 months.
Showing 8041–8060 of 48,215 recalls
Recalled Item: Baxter Epiphany Cardio Server E3 ECG Management System Servers with Recalled...
The Issue: Epiphany, now a Baxter Healthcare company, is issuing an Urgent Medical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veran:SPiN Thoracic Navigation System Models: SYS-4230 SPiN Thoracic...
The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn Connex Spot Monitor Recalled by Baxter Healthcare Corporation...
The Issue: Product is being recalled due to the improper placement of a copper tape on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Marquee Disposable Core Biopsy Instrument Kit Recalled by Bard...
The Issue: Diameter mismatch between coaxial and biopsy needle (cutting cannula) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow ErgoPack Pressure Injectable One-Lumen PICC Recalled by ARROW...
The Issue: This recall has been initiated due to reports that the product code and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veran : Endobronchial Always on Track Models: INS-0392 AOTT 21ga Needle...
The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow ErgoPack Recalled by ARROW INTERNATIONAL Inc. Due to This recall has...
The Issue: This recall has been initiated due to reports that the product code and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Guardian 2 System Product Name: Guardian System 2 Recalled by...
The Issue: A software update corrected an issue where "low" and "terminal" battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proboscis/Piston Assembly Recalled by Ortho-Clinical Diagnostics, Inc. Due...
The Issue: Ortho Clinical Diagnostics (QuidelOrtho) confirmed certain Proboscis/Piston...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALCOLADO RELAMPAGO (Menthol and Camphor) Recalled by Ecometics, Inc. Due to...
The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blis-To-Sol Liquid (Tolnaftate) Recalled by Ecometics, Inc. Due to CGMP...
The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Unguentine Ointment Recalled by Ecometics, Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: YAGER'S LINIMENT (Camphor and Turpentine Oil) 3.1% and 8.12% respectively...
The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: activator concentrate Recalled by Ecometics, Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lugol's (Strong Iodine Solution USP) Recalled by Ecometics, Inc. Due to CGMP...
The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AstrinGyn (Ferric Subsulfate) Aqueous Recalled by Ecometics, Inc. Due to...
The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Butter Flavored Popcorn Naturally & Artificially Flavored Recalled by...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 10ML SYRINGE LUER LOCK W/OUT NEEDLE Recalled by Fresenius Medical Care...
The Issue: There is a potential for blood backfill leakage and foreign material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Pentacam AXL Wave Recalled by Oculus Optikgeraete GMBH Due to Their...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Myopia Master Recalled by Oculus Optikgeraete GMBH Due to Their is a...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.