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. 2,608 recalls have been distributed to Nebraska in the last 12 months.
Showing 9961–9980 of 28,140 recalls
Recalled Item: EASYNJECT Recalled by BIOPSYBELL S.R.L. Due to Products labeled as sterile...
The Issue: Products labeled as sterile were distributed, but may not have been sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10G COAXIAL CANNULA WITH TUOHY CONNECTION Recalled by BIOPSYBELL S.R.L. Due...
The Issue: Products labeled as sterile were distributed, but may not have been sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 GAUGE CEMENT DELIVERY CANNULA Recalled by BIOPSYBELL S.R.L. Due to...
The Issue: Products labeled as sterile were distributed, but may not have been sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CEMIX - CEMENT MIXING SYSTEM Recalled by BIOPSYBELL S.R.L. Due to Products...
The Issue: Products labeled as sterile were distributed, but may not have been sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11G DIRECT WORKING CANNULA DIAMOND TIP MINI Recalled by BIOPSYBELL S.R.L....
The Issue: Products labeled as sterile were distributed, but may not have been sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue IABP - Product Usage: used to inflate and Recalled by...
The Issue: There are cybersecurity vulnerabilities in a widely used low-level TCP/IP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid IABP - Product Usage: used to inflate and Recalled by...
The Issue: There are cybersecurity vulnerabilities in a widely used low-level TCP/IP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL470...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NO156Z...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL494...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NO180Z...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL476...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System Tray Sysem knee implant devices as follows: Recalled by...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL488...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL482...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution CT Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential issue on the Revolution CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer - Product Usage: intended to assist in the...
The Issue: When the Cross Enterprise Display option is enabled on the Centricity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interventional Fluoroscopic X-Ray System ARTIS icono biplane- 11327600 ARTIS...
The Issue: Siemens has become aware of a potential issue with software version VE20C....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protek Solo Venous Dilator Set: dilator Recalled by Cardiac Assist, Inc Due...
The Issue: On 02/26/2021, it was found that there were incorrectly packaged Dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chromosome X Alpha-Satellite in FITC Spectrum - Product Usage: Analyte...
The Issue: Users may observe additional locus specific signals at 9q34. The device pack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.