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. 2,650 recalls have been distributed to Nebraska in the last 12 months.
Showing 1461–1480 of 28,140 recalls
Recalled Item: Brand Name: Osteotec Product Name: Osteotec Silicone Finger Implant...
The Issue: There is the potential that the silicone implant may contain foreign material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink SmartSync Patient Connector Recalled by Medtronic, Inc....
The Issue: In prior SmartSync application versions, the Abort button stopped the test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Due to complaints their is...
The Issue: Due to complaints their is the potential that irrigation solution may leaked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink SmartSync Device Manager Recalled by Medtronic, Inc. Due...
The Issue: In prior SmartSync application versions, the Abort button stopped the test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Due to complaints their is...
The Issue: Due to complaints their is the potential that irrigation solution may leaked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickVue: Dipstick Strep A Test: 50T Recalled by Quidel Corporation Due to...
The Issue: Dipstick strep A test has potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MI Cancer Seek UDI Code: (01)00860008613325(21)H5HJHDSXF MI Cancer Recalled...
The Issue: Due to an incorrect test results provided that indicated the incorrect drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SwabFlush Prefilled Syringe with ICU Medical SwabCaps Recalled by MEDLINE...
The Issue: SwabFlush syringes are affected by the ICU Medical recall of their SwabCap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PhaSeal Injector Luer (N30C) Recalled by BD SWITZERLAND SARL Due to...
The Issue: Closed system drug transfer devices were shipped to the U.S. market without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeStar 90 Plus Filter. Bidirectionally breathing system filter. Recalled...
The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeStar 55 Plus Filter. Bidirectionally breathing system filter. Recalled...
The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeStar 60A Plus Filter. Bidirectionally breathing system filter. Recalled...
The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HME TwinStar HEPA Plus Filter. Bidirectionally breathing system filter....
The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biofinity XR Toric Contact Lens Recalled by CooperVision, Inc. Due to Lens...
The Issue: Lens blisters may have an incomplete or leaking seal which may render them...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biofinity Toric Multifocal Contact Lens Recalled by CooperVision, Inc. Due...
The Issue: Lens blisters may have an incomplete or leaking seal which may render them...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Visions Digital IVUS Catheter: PV.014P (Platinum) Recalled by...
The Issue: Reports of IVUS catheter and guide wire entanglement during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estrone RIA Catalog Number DSL8700 UDI Code: 15099590211615 Estrone RIA...
The Issue: Estrone RIA kit lots may rarely give falsely high patient results which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL Recalled by Johnson & Johnson Vision...
The Issue: Due to defects (bubbles/voids) identified during standard finished goods testing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products OP Reagent Gen 15. Model Number: 680 Recalled by...
The Issue: Lots from Generation (GEN) 15 of VITROS Chemistry Products OP Reagent may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASPRIRE Cristalle Mammography System (cleared under K212873) installed with...
The Issue: Devices had an unapproved slabbing software function enabled for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.