Product Recalls in Nebraska
Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,455 recalls have been distributed to Nebraska in the last 12 months.
Showing 23141–23160 of 49,150 recalls
Recalled Item: Montmorency Tart Cherry Concentrate 100% Juice 32-oz bottle (sold individual...
The Issue: Incorrect quantity of sugar listed in Nutrition Facts. Label states 1g sugar...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vacuum Unit for CATSmart Vacuum Pump. Fresenius CATSmart (Continuous...
The Issue: The optional Vacuum Unit may stop working and display the failure message...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Blue Line Ultra Tracheostomy Tube Inner Cannula. One cannula Recalled...
The Issue: Packaged with an incorrect size inner cannula.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith Medical JELCO Hypodermic Needle-Pro EDGE Safety Device Safety Device...
The Issue: Incorrect needle length and gage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Delta Family patient monitors The Infinity Delta Series...
The Issue: The firm is recalling their Delta family of patient monitors software due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 Uroskop...
The Issue: The swivel arm holding the monitors may become dislodged from the carrying arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omega Systems These devices are intended to be used in Recalled by Draegar...
The Issue: The firm is recalling their Delta family of patient monitors software due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiohelp Emergency Drive Recalled by Maquet Cardiovascular Us Sales, Llc...
The Issue: Upon servicing the gearwheel in the Emergency Drive the gearwheel may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia -fluoroscopic X-ray system Model # 10094910 The Uroskop...
The Issue: The swivel arm holding the monitors may become dislodged from the carrying arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinix DP- i(Infinix-8000F) CAT-870B Catheterization Table (Titling) -...
The Issue: Table tilts without operator involvement as a result of liquid spilling into...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Watermelon Recalled by World Waters, LLC dba WTRMLN WTR Due to Cold Pressed...
The Issue: Cold Pressed Juice Watermelon WTRMLN WTR Original 12 packs due to the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Life-Line tm Catalytic Activated Energy Water Recalled by McDaniel Life-Line...
The Issue: Unapproved new drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Indian Herb Paste (a dietary supplement) Ingredients: Galangal Recalled by...
The Issue: Unapproved new drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mometasone Furoate Cream Recalled by ACP Nimble Buyer, Inc. Due to Labeling:...
The Issue: Labeling: Not Elsewhere Classified. Mometasone Furoate Cream has an NDC...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DG Baby Gripe Water herbal supplement with organic ginger and fennel...
The Issue: Presence of an undissolved ingredient, citrus flavonoid.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: Recalled...
The Issue: Frayed pieces of the mounting card being inside the primary packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medica Wash1-Wash solution used prior to Lipase assay on the Recalled by...
The Issue: Wash1 solution is ineffective in cleaning dispensing probe of TRIG and LDL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LW Scientific ZIP IQ Combo Centrifuge Recalled by LW Scientific, Inc. Due to...
The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LW Scientific ZIP IQ Combo Centrifuge Recalled by LW Scientific, Inc. Due to...
The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LW Scientific ZIP IQ PCV Centrifuge Recalled by LW Scientific, Inc. Due to...
The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.