Nebraska Recalls
3,135 recalls on record affecting Nebraska
Nutricia North America recalls functional formularies NOURISH ORGANIC WHOLE FOODS MEAL REPL
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.
View recall details →
Nutricia North America recalls functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.
View recall details →
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS,
Due to packaging discrepancy with incorrect product size mixed up.
View recall details →
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS,
Due to packaging discrepancy with incorrect product size mixed up.
View recall details →
MARS SNACKING recalls MorningStar Farms Hot & Spicy Sausage Patties, 100% Plant Pr
Potential contamination with plastic material
View recall details →
MARS SNACKING recalls MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein
Potential contamination with plastic material
View recall details →
Beta Bionics, Inc. recalls iLet Bionic Pancreas, REF: BB1001
The reason for the recall is: it was found in version 3.3.6 of the iLet ACE Pump firmware and all previous releases that a screen unlock failure could occur when the user successfully slides the unlock slider on the Lock Screen, no screen transition occurs, and the user remains on the Lock Screen. Because the user cannot exit the Lock Screen, the user is unable to perform a cartridge change or meal announcement. If this occurs and therapy is in progress, therapy will continue normally until the insulin cartridge is depleted. The user will be unable to perform a cartridge change or a meal announcement and will be stuck on the screen until the battery fully drains. This can lead to hyperglycemia.
View recall details →
BD SWITZERLAND SARL recalls BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382
Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening securely. This behavior has led some clinical users to perceive the connection as unstable.
View recall details →
Abiomed, Inc. recalls Impella CP Set with SmartAssist. Product Codes: 1000080, 100
Exposure to the low purge pressure occurrence may result in persistent low purge pressure alarms and, in some cases, interruption or loss of mechanical circulatory support.
View recall details →
Nutrisystem Inc recalls Nutrisystem, Chocolate Cheesecake, 2 oz (57g) packages, Flow
Undeclared Allergen (Soy)
View recall details →
United States Bakery recalls Great Value Hawaiian Roll 4pk, Item # F63384. Product is per
Firm observed oily and sticky substance on direct food contact surface packaging of finished product.
View recall details →
U.S. Tov, Inc. dba U.S. Trading Company recalls DRAGONFLY Thai Ginger Powder Net Weight: 4.37 oz (125 g) PRO
Potential contamination with lead.
View recall details →
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 →
The Coffee Connexion Co., Inc recalls Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag a
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
View recall details →
The Coffee Connexion Co., Inc recalls Alfredo Sauce, 3 lb. 7 oz., packaged in a sealed poly bag an
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
View recall details →
The Coffee Connexion Co., Inc recalls 1) Cheese Sauce Mix, 25.5 oz., packaged in a sealed poly bag
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
View recall details →
The Coffee Connexion Co., Inc recalls Aramark Cheese Sauce New & Improved, 25 lb., packaged in a t
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
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 →
Pork King Good, LLC recalls Pork King Good Onion & Sour Cream Seasoning. Net Wt. 3 oz (
Seasoning was made with recalled California Dairies milk powder due to Salmonella contamination.
View recall details →
Showing 20 of 3,135 recalls. Use search to filter further.