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. 2,630 recalls have been distributed to Nebraska in the last 12 months.
Showing 4621–4640 of 28,140 recalls
Recalled Item: Thermalon Sinus Compress Recalled by Bruder Healthcare Company, LLC Due to...
The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermalon Stye Compress Recalled by Bruder Healthcare Company, LLC Due to...
The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYRINGE Recalled by Alcon Research, LLC Due to Medline Bulb irrigation...
The Issue: Medline Bulb irrigation syringes recalled due to potential for packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermalon Neck Wrap Recalled by Bruder Healthcare Company, LLC Due to...
The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFlock Sterile Flocked Collection Device Recalled by Puritan Medical...
The Issue: It was discovered through a customer complaint that mislabeled product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediBeads Neck Wrap Recalled by Bruder Healthcare Company, LLC Due to...
The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermalon Eye Compress Recalled by Bruder Healthcare Company, LLC Due to...
The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediBeads King Pad Recalled by Bruder Healthcare Company, LLC Due to...
The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermalon Heating Pad Recalled by Bruder Healthcare Company, LLC Due to...
The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nimbus Administration Set Recalled by InfuTronix LLC Due to InfuTronix is...
The Issue: InfuTronix is removing the Nimbus Infusion Pump Systems from the market due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nimbus II Infusion System Recalled by InfuTronix LLC Due to InfuTronix is...
The Issue: InfuTronix is removing the Nimbus Infusion Pump Systems from the market due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Situate Laparotomy Sponge Recalled by Covidien Due to Packs including 5...
The Issue: Packs including 5 laparotomy sponges may contain incorrect product with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20 Fr Safety PEG Push w/ENFit Kit (Box 2)-Indicated Recalled by...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Standard PEG Kit w/ENFit (Box 2)-Indicated for Recalled...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Safety PEG Kit w/ENFit (Box 2)-Indicated for Recalled by...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Standard PEG Kit (Box 2)-Indicated for enteral Recalled...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Safety PEG Kit (Box 2)-Indicated for enteral Recalled by...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HALYARD SURGICAL HOOD Recalled by O&M HALYARD, INC. Due to Mislabeling
The Issue: Product was mislabeled as a Surgical Cap at its dispenser level.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiovascular Procedure Kits that include High Crack Check Valve PN...
The Issue: Pressure relief valve included in certain lots of cardiovascular procedure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Tube Securement Device Recalled by 3M Company - Health Care Business Due...
The Issue: Manufacturing nonconformities are in some lots of the Tube Securement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.