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 5221–5240 of 28,140 recalls
Recalled Item: Medline Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...
The Issue: Medline Industries, LP is recalling certain kits and trays that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...
The Issue: Medline Industries, LP is recalling certain kits and trays that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...
The Issue: Medline Industries, LP is recalling certain kits and trays that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ARTERIAL BUNDLE NO CATHETER Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medline Industries, LP is recalling certain kits and trays that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Medline Industries, LP is recalling certain kits and trays that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...
The Issue: Medline Industries, LP is recalling certain kits and trays that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE kits and trays Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Medline Industries, LP is recalling certain kits and trays that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOHELP-i Heart Lung Support System: Blood oxygenation and carbon dioxide...
The Issue: CARDIOHELP-i System was not properly tested to measure leakage current
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Recanalization System Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: Recanalization systems may be in a manufacturing mode that allows the system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hookup Accessories used with MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS...
The Issue: Identification label on affected hookups could become illegible over time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calibration Serum Level 3. CAL 3 Recalled by Randox Laboratories Ltd. Due to...
The Issue: There have been transcription errors on the Instructions For Use (IFU) of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous probe connection cable ( and 701048804) used with Recalled by Maquet...
The Issue: Firm received complaints of breaks in the insulation, shielding, or wires of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORI REAL INTELLIGENCE Robotic Drill Recalled by Blue Belt Technologies, Inc...
The Issue: Possibility that the user is unable to resolve drill disconnection error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20IN (50.8CM) BRAIDED INJ LINE Recalled by Smiths Medical Asd Inc Due to...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO surgical EMPOWR Porous Knee System Empowr 3D Femur-Porous Coated...
The Issue: Due to incorrect product/device within packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 18-19-20. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 8.5-9.5-10.5. indicated for endoscopic dilation...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 11-12-13. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 11-12-13. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 8.5-9.5-10.5. Indicated for endoscopic dilation...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.