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. 2,466 recalls have been distributed to Nebraska in the last 12 months.
Showing 21641–21660 of 28,140 recalls
Recalled Item: Covidien Argyle Infant Heel Warmers (no tab) Item Code: MH00002N Recalled by...
The Issue: Infant Heel warmers may break during activation resulting in spillage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Argyle Infant Heel Warmers (with tab) Item Code: MH00002T Recalled...
The Issue: Infant Heel warmers may break during activation resulting in spillage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Symbia S Series system Recalled by Siemens Medical Solutions USA,...
The Issue: Fuses with the improper amperage rating were installed in the Symbia S,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Pressure Monitoring Kit with TruWave disposable pressure transducer....
The Issue: Flow restriction issues in a trifurcated IV set included in the pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Voyant Open Fusion Device Models: EB040 and EB040+ Product Usage: Recalled...
The Issue: Potential to improperly characterize tissue within the jaws, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Symbia T Series Recalled by Siemens Medical Solutions USA, Inc. Due...
The Issue: Fuses with the improper amperage rating were installed in the Symbia S,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Intevo Series system Recalled by Siemens Medical Solutions USA, Inc....
The Issue: Fuses with the improper amperage rating were installed in the Symbia S,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow International Recalled by Arrow International Inc Due to saline...
The Issue: saline leakage from unsecured connections between the Touhy Borst adaptor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU680 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman coulter has received complaints regarding leaking and cracked C...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU5800 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman coulter has received complaints regarding leaking and cracked C...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PICC Kits with Peel-Away Sheath Component Recalled by Arrow International...
The Issue: the catheter peel-away component hub tabs may prematurely detach. One injury...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU480 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman coulter has received complaints regarding leaking and cracked C...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Multi-Access Port Closed Suction System for Adults Recalled by...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Multi-Access Port Replacement Catheter for Adults Recalled by...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Wet Pak* Closed Suction System for Adults Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Wet Pak* Closed Suction System for Adults Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.