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. 988 recalls have been distributed to Nebraska in the last 12 months.
Showing 34781–34800 of 49,150 recalls
Recalled Item: CPT 12/14 COCR prosthesis Recalled by Zimmer Biomet, Inc. Due to LDPE bag...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NKII CSTI Porous Femoral NKII NP Femoral prosthesis Recalled by Zimmer...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specify 5-6-5 Lead Recalled by Medtronic Neuromodulation Due to Some Specify...
The Issue: Some Specify 5-6-5 and 2x8 surgical lead product labeling does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bipolar Shell prosthesis Recalled by Zimmer Biomet, Inc. Due to LDPE bag...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BEAVER Blade 4.0mm Part Number: 72203307 Orthopedic Recalled...
The Issue: Blade exhibiting fracture during hip arthroscopy procedures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS 6 INCH BEADED FC 1 prosthesis Recalled by Zimmer Biomet, Inc. Due to...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRCT MIS CR MOB PLT prosthesis Recalled by Zimmer Biomet, Inc. Due to LDPE...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CR Flex GSF Porous Femoral LPS Flex GSF Porous Femoral Recalled by Zimmer...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS-FLEX GSF OPT prosthesis Recalled by Zimmer Biomet, Inc. Due to LDPE bag...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Knee LPS Porous FEM NexGen Knee LPS Option FEM Recalled by Zimmer...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZIMMER UNI HIGH FLEX PRECOAT FEM prosthesis Recalled by Zimmer Biomet, Inc....
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gender PFJ FEMORAL COMP Recalled by Zimmer Biomet, Inc. Due to LDPE bag...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse Treatment Planning System versions 11 Recalled by Varian Medical...
The Issue: When using PBC 11.0.31 to calculate the dose for a conventional arc field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lyrica (pregabalin) capsules Recalled by Pfizer Inc. Due to FAILED...
The Issue: FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lyrica (pregabalin) capsules Recalled by Pfizer Inc. Due to FAILED...
The Issue: FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Black Ant King Recalled by R Thomas Marketing, LLC Due to Marketed Without...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zhong Hua Niu Bian Recalled by R Thomas Marketing, LLC Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Samurai-X Recalled by R Thomas Marketing, LLC Due to Marketed Without An...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bull's Genital Recalled by R Thomas Marketing, LLC Due to Marketed Without...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bull Recalled by R Thomas Marketing, LLC Due to Marketed Without An Approved...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.