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. 2,362 recalls have been distributed to Nebraska in the last 12 months.
Showing 1161–1180 of 28,140 recalls
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Radiology Solutions software version 14.2.2 Recalled by...
The Issue: Due to software issue, radiology reports may not be fully displayed when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 900 COULTER Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Hematology analyzers configured with HGB photometers may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 690T COULTER Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Hematology analyzers configured with HGB photometers may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to a faulty electrical connection between the speed control Dial and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to a faulty electrical connection between the speed control Dial and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Pheno. Image-Intensified Flouroscopic X-Ray System. Recalled by...
The Issue: Limited system movements after startup .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to a faulty electrical connection between the speed control Dial and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...
The Issue: Their is the potential for weak staining which may result in false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...
The Issue: Their is the potential for weak staining which may result in false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Hemo Recalled by Merge Healthcare, Inc. Due to Merge Healthcare has...
The Issue: Merge Healthcare has been informed by Schiller AG (Baar, Switzerland) of an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...
The Issue: Their is the potential for weak staining which may result in false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP). Material Number:...
The Issue: Potential for falsely depressed patient, quality control (QC), and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baster Continu-Flo Solution Set Recalled by Baxter Healthcare Corporation...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Cardiovascular Recalled by Philips Medical Systems Nederland...
The Issue: Software issue that results in the display of outdated information.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2% Recalled...
The Issue: Blood collection tubes were manufactured with the label applied too high on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.