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. 2,650 recalls have been distributed to Nebraska in the last 12 months.
Showing 1121–1140 of 28,140 recalls
Recalled Item: Venclose digiRF Generators Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: Software version 3.35 of the Venclose digiRF Generator incorporates a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT EG6+ cartridge. List Number: 03P77-25. Recalled by Abbott Point Of...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT CG4+ cartridge (white). List Number: 03P85-25. Recalled by Abbott...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG4+ cartridge to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT CG8+ cartridge. List Number: 03P88-25. 510(k) numbers: K894914...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT EG7+ cartridge. List Number: 03P76-25. Recalled by Abbott Point Of...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MST ArcDUO 9mm Recalled by MicroSurgical Technology Inc Due to An ophthalmic...
The Issue: An ophthalmic knife has a suction set (not direct patient-contacting), which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CorNeat EverPatch Recalled by CORNEAT VISION, LTD. Due to Reviewed...
The Issue: Reviewed complaints have identified that conjunctival wound dehiscence may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EverPatch+ Recalled by CORNEAT VISION, LTD. Due to Reviewed complaints have...
The Issue: Reviewed complaints have identified that conjunctival wound dehiscence may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICEfx Cryoablation System Recalled by Boston Scientific Corporation Due to...
The Issue: Certain desiccant tube subassemblies were built with end caps that were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preventive Maintenance (PM) Kit ICEFX Recalled by Boston Scientific...
The Issue: Certain desiccant tube subassemblies were built with end caps that were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartstring III Proximal Seal System. Intravascular anastomosis occluder....
The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017 Recalled by...
The Issue: Potential for activation of an abnormal alarm pause.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device...
The Issue: Potential for barb non-engagement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe Recalled by Exactech, Inc. Due to Reverse Shoulder humeral...
The Issue: Reverse Shoulder humeral liners have an articular surface position outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.