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. 2,479 recalls have been distributed to Nebraska in the last 12 months.
Showing 20981–21000 of 28,140 recalls
Recalled Item: MOSAIQ Oncology Information System MOSAIQ is an oncology information system...
The Issue: Incorrect drug dosage due to "Age Limit" and patient weight data item issue.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 2-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer ClWIZARD2 5-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM systems Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Possible installation error of the quench lines of superconducting magnets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model NuCARTGN. The NuCART is a mobile display and image Recalled by...
The Issue: The attachment of the NuCART Spring Arm to the NuCART horizontal boom may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quick Connects. Steris Corporation. Model numbers: QKC1736E Recalled by...
The Issue: The firm discovered that one of the hysteroscope models listed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.