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. 1,005 recalls have been distributed to Nebraska in the last 12 months.
Showing 27121–27140 of 49,150 recalls
Recalled Item: LPS-FLEX PRECOAT FEMORAL B-R LPS-FLEX PRECOAT FEMORAL C-L LPS-FLEX PRECOAT...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CR PRECOAT FEM COMP SIZE BMR CR PRECOAT FEM COMP Recalled by Zimmer Biomet,...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIPOLAR METAL SHELL 48 MM OD Use of the MultiPolar Recalled by Zimmer...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FEM PRC LT M/RT L SML FEM PRC RT M/LT Recalled by Zimmer Biomet, Inc. Due to...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS-FLEX GSF OPT SZ C-L¿ LPS-FLEX GSF OPT SZ C-R¿ Recalled by Zimmer Biomet,...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CR-FLEX POR HATCP FEM C-L CR-FLEX POR HATCP FEM C-R Recalled by Zimmer...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CR OPTION FEM COMP SIZE C/L CR OPTION FEM COMP Recalled by Zimmer Biomet,...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS PRECOAT FEM SIZE D-RT LPS PRECOAT FEM SIZE E-RT Recalled by Zimmer...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS 6 INCH BEADED FC 13X160MM LM BODY EXT NECK & STD NECK Prosthesis...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT 12/14 COCR SIZE 0 STD prosthesis Recalled by Zimmer Biomet, Inc. Due to...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered Screw-Vent MTX Recalled by Zimmer Dental Inc Due to Mislabeling
The Issue: Two lots of the Tapered Screw-Vent Implants, with different outer thread...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered Screw-Vent MTX Recalled by Zimmer Dental Inc Due to Mislabeling
The Issue: Two lots of the Tapered Screw-Vent Implants, with different outer thread...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee spacer block instruments Recalled by Zimmer Biomet,...
The Issue: Certain partial knee implant spacer blocks do not fit in the alignment tower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penicillin V Potassium for Oral Solution Recalled by Teva Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: high out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vertra Elemental Resistance (Octyl Methoxycinnamate 6% Recalled by EAI-JR286...
The Issue: CGMP Deviations: products manufactured in a manner that may impact product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DERMABOND" PRINEO" Skin Closure System Product Usage: DERMABOND PRINEO...
The Issue: Ethicon discovered that specific lots of DERMABOND"PRINEO"System may not dry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm¿ Dual Reservoir Cooler/Heater System Models 400CE and 400MR...
The Issue: Due to FDA's safety communication relating to nontuberculous mycobacteria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syva¿ EMIT¿ 2000 Theophylline Product Usage: The Syva¿ Emit¿ 2000 Recalled...
The Issue: Lot J1 of the Syva¿ EMIT¿ 2000 Theophylline Assay, when run on a Beckman AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peanut Delight (8 oz. bag) Recalled by Colorado Nut Co Due to Undeclared Milk
The Issue: Undeclared milk in snack mix products
Recommended Action: Do not consume. Return to store for a refund or discard.