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. 1,025 recalls have been distributed to Nebraska in the last 12 months.
Showing 21381–21400 of 49,150 recalls
Recalled Item: DEMO No Needle Corrugated Carton 40 U/D Recalled by Valeritas, Incorporated...
The Issue: There is a potential for "No Needle Demo Units" to contain a needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEMO No Needle Corrugated Carton 30 U/D Recalled by Valeritas, Incorporated...
The Issue: There is a potential for "No Needle Demo Units" to contain a needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPECTRALIS with HEYEX2 image management system. a non-contact ophthalmic...
The Issue: Error in the default configuration which could lead to the incorrect display...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Drive Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEMO No Needle Corrugated Carton 20 U/D Recalled by Valeritas, Incorporated...
The Issue: There is a potential for "No Needle Demo Units" to contain a needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LivaNova SMART PERFUSION PACK INSPIRE 8S - Product Usage: The Recalled by...
The Issue: Perfusion tubing pack was packaged with the incorrect cuvette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CapsoCam Plus *** System Recalled by Capso Vision, Inc. Due to Possible...
The Issue: Possible mis-labeling of the device with incorrect serial number labels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Confidence Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEMO No Needle Corrugated Carton 30 U/D Recalled by Valeritas, Incorporated...
The Issue: There is a potential for "No Needle Demo Units" to contain a needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEMO No Needle Corrugated Carton 20 U/D Recalled by Valeritas, Incorporated...
The Issue: There is a potential for "No Needle Demo Units" to contain a needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Tina-Quant Myoglobin Gen. 2 Tests system is an immuno-turbidimetric...
The Issue: The firm conducted internal investigations that confirmed customer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAsymphony SP SOW 5.0.3 Recalled by Qiagen Sciences LLC Due to QIAsymphony...
The Issue: QIAsymphony software version 5.0.3 - Software issue incorreclty assigns the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blanketrol III Hyper-Hypothermia System- body hypothermia system temperature...
The Issue: Warnings statements have been added- exceeding 40 degree C for extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blanketrol II Hyper-Hypothermia System Recalled by Cincinnati Sub-Zero...
The Issue: Warnings statements have been added- exceeding 40 degree C for extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoolBlue Hyper-Hypothermia System- body hypothermia system Model: Innercool...
The Issue: Warnings statements have been added- exceeding 40 degree C for extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grandall Colirio Ojo De Aguila Eye Drops Recalled by Altaire...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.