- Home
- Idaho Recalls
Idaho Recalls
2,405 recalls on record affecting Idaho
Fresenius Kabi USA, LLC recalls Ivenix Infusion System (IIS), Large Volume Pump, Model Numbe
Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components that may not be apparent or readily visible and the devices therefore remained in service. More specifically, drops or jarring on a hard surface can cause the touchscreen input cable to loosen, resulting in unintended touchscreen behavior on the LVP, including random screen touches and/or lack of screen responsiveness to user input. Under the reported failure condition, unintended touch inputs may register at arbitrary screen locations without user interaction. These inputs occur intermittently and without a predictable pattern.
View recall details →
Intuitive Surgical, Inc. recalls Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000
Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching from the handheld camera to the robotic endoscope.
View recall details →
C.R. Bard Inc recalls Silastic Foley Catheters Silastic Brand Foley Catheter 30cc
Due to stain present on the surface of affected foley catheters.
View recall details →
Ghirardelli Chocolate Company recalls GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED
Potential contamination with Salmonella.
View recall details →
Ghirardelli Chocolate Company recalls GHIRARDELLI PREMIUM HOT COCOA MIX NET WT 32oz (2lbs) 907g In
Potential contamination with Salmonella.
View recall details →
Ghirardelli Chocolate Company recalls GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX MOCHA NET WT 50oz (
Potential contamination with Salmonella.
View recall details →
Ghirardelli Chocolate Company recalls GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CLASSIC WHITE NET W
Potential contamination with Salmonella.
View recall details →
Ghirardelli Chocolate Company recalls GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED
Potential contamination with Salmonella.
View recall details →
Ghirardelli Chocolate Company recalls GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX VANILLA NET WT 48oz
Potential contamination with Salmonella.
View recall details →
Ghirardelli Chocolate Company recalls GHIRARDELLI SWEET GROUND POWDER CHOCOLATE & COCOA NET WT 48o
Potential contamination with Salmonella.
View recall details →
Ghirardelli Chocolate Company recalls GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX WHITE MOCHA NET WT
Potential contamination with Salmonella.
View recall details →
Ghirardelli Chocolate Company recalls GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX FROZEN HOT COCOA NE
Potential contamination with Salmonella.
View recall details →
Ghirardelli Chocolate Company recalls GHIRARDELLI SWEET GROUND POWDER WHITE CHOCOLATE FLAVORED NET
Potential contamination with Salmonella.
View recall details →
Elekta, Inc. recalls Brand Name: Leksell Vantage Arc System REF: 1053958
Locking mechanisms may not properly secure to the Arc system, resulting in shifting of coordinates during procedures.
View recall details →
Marquez Brothers International, Inc. recalls EL MEXICANO horchata casera Instant Horchata Drink NET WT 14
Undeclared milk.
View recall details →
Marquez Brothers International, Inc. recalls EL MEXICANO agua fresca de horchata Instant Horchata Drink N
Undeclared milk.
View recall details →
Marquez Brothers International, Inc. recalls Bulk Horchata Powder 3951 (100547) 1/25 HORCHATA UPC: 0427
Undeclared milk.
View recall details →
Stryker Sustainability Solutions recalls Stryker Sustainability Solution Color Cuff 24" (Yellow) Quic
Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.
View recall details →
Brahms GmbH recalls B.R.A.H.M.S PlGF Plus KRYPTOR, Catalog Number: 859075N. in
Customers have observed quality control values out of range at the lowest quality control level (QC Level 1) for the PIGF assay which require troubleshooting steps to resolve. If Quality Controls are not performed according to the Instructions for Use, the underestimation of QC1 may go undetected and could contribute to falsely elevated sFlt-1/PlGF ratio results. A falsely elevated sFlt-1/PlGF ratio may result in a higher-risk classification for progression to preeclampsia with severe features potentially leading to intensified clinical monitoring.
View recall details →
Exactech, Inc. recalls Brand Name: Equinoxe Product Name: Equinoxe Core Instrumen
Impactor handle may be missing cross-pin
View recall details →
Showing 20 of 2,405 recalls. Use search to filter further.