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. 2,612 recalls have been distributed to Nebraska in the last 12 months.
Showing 9041–9060 of 28,140 recalls
Recalled Item: OPTETRAK LOGIC Polyethylene Tibial Inserts Recalled by Exactech, Inc. Due to...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTHROFOCUS Polyethylene Tibial Inserts (Product Line: 256-12-XX Recalled by...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vantage Total Ankle System including a. Vantage Fixed-Bearing Polyethylene...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRULIANT Knee System including TRULIANT Tibial Inserts Recalled by Exactech,...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System custom devices labeled as the following:...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System Recalled by Exactech, Inc. Due to Inserts...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK All-polyethylene UNI...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK Logic RBK PS Tibial...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software BeamAdjust version 2.2 Recalled by PTW NORTH AMERICA CORPORATION...
The Issue: When a measurement with a PTW detector array is performed with the software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part...
The Issue: Due to product not meeting specification for concentricity and failing to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EcoLotion Transmission Lotion Recalled by North Coast Medical Inc Due to...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norco Ultrasound Gel Recalled by North Coast Medical Inc Due to Ultrasound...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Pneumostat Chest Drain Valve Recalled by Atrium Medical Corporation...
The Issue: The firm is revising the Indication for Use, Contraindications, Warnings,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...
The Issue: Labeled On-board instrument stability issue for current and future lots,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Liquid Anti-Xa- automated chromogenic assay for in vitro diagnostic...
The Issue: Labeled On-board instrument stability issue for current and future lots,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...
The Issue: Labeled On-board instrument stability issue for current and future lots,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium ADVANTA VXT Vascular Graft Recalled by Atrium Medical Corporation Due...
The Issue: The product package may potentially contain a mismatched graft that does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.