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. 2,439 recalls have been distributed to Nebraska in the last 12 months.
Showing 25481–25500 of 28,140 recalls
Recalled Item: DRX Revolution Mobile X-Ray System Recalled by Carestream Health, Inc. Due...
The Issue: During an audit, Carestream discovered a DRX-1 System that captured an image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atlas Spine Torque Limiting Handle 6N-m Recalled by Atlas Spine, Inc. Due to...
The Issue: The device was not appropriately set to mitigate the risk of implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT cobas 4800 HPV AMP/DET 240T / 960T US-IVD Recalled by Roche Molecular...
The Issue: During an internal investigation, a formulation error that occurred was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DICOM Export Format for Sum Dose with Velocity v3.0.0. A Recalled by...
The Issue: An anomaly was detected such that, under certain conditions, a summed dose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemoCue¿ Hb 201 Microcuvettes Recalled by HemoCue AB Due to HemoCue AB has...
The Issue: HemoCue AB has become aware of a production related problem involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic O-arm Imaging System Mobile X-ray system. Model No. BI-700-00027...
The Issue: Review of on-system electronic product labeling and Instructions for comply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 100NX Cassettes Recalled by Advanced Sterilization Products Due to...
The Issue: The recall of the STERRAD 100NX Cassettes was initiated because Advanced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nestle Nutrition Recalled by Nestle HealthCare Nutrition Due to Nestle...
The Issue: Nestle HealthCare Nutrition, Inc. is initiating a recall on some of Compat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GYRUS ACMI Recalled by Gyrus Medical, Inc Due to On April 29, 2013 Olympus...
The Issue: On April 29, 2013 Olympus Surgical Technologies America R&D received results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2mm Drill Bit. This is a component within the PediLoc Recalled by...
The Issue: OrthoPediatrics has initiated a voluntary recall of Part # 01-1050-002,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stereotactic Circular Collimator - 3D Line stereotatic Hardware Accessories...
The Issue: Potential for clinical errors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contra-Angle Torque Driver Kit For Certain and External Connection Product...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense...
The Issue: The firm issued a clinical alert after users reported an issue where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered Navigator Certain Surgical Kit Product Usage: Molded plastic tray...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.7mm and 5.0mm Dynamic Locking Screw (DLS) Product Usage: 3.7mm Recalled by...
The Issue: All lots of 3.7mm and 5.0mm Dynamic Locking Screw (DLS) were recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contra-Angle Torque Driver Kit Product Usage: Molded plastic tray used...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigator Surgical Kit Product Usage: Molded plastic tray used in Recalled...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contra-Angle Torque Driver Kit For Certain Internal Connection Product...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP (Base) Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential carryover issue that can can cause shortened APTT clotting times...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 300 and ACL TOP 300 CTS (Japan) Recalled by Instrumentation...
The Issue: Potential carryover issue that can can cause shortened APTT clotting times...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.