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. 2,450 recalls have been distributed to Nebraska in the last 12 months.
Showing 23601–23620 of 28,140 recalls
Recalled Item: ACL Sleeve Installation Tool Sizes: 6mm Recalled by OrthoPediatrics Corp Due...
The Issue: Weld fractures on the Sleeve Installation Tool for ACL reconstruction system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GALT VALVED TEARAWAY KIT GALT VTI w/ Sideport Stainless Steel Recalled by...
The Issue: The adhesive used in the product could dislodge when objects are inserted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker T2 Tibia System Nail Insertion Sleeve Recalled by Stryker Howmedica...
The Issue: Stryker Orthopaedics received a report indicating some of the Nail Insertion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VER2 D8L OFFSET RASP HANDLE Recalled by Zimmer, Inc. Due to The firm...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VER2 HANDLE Recalled by Zimmer, Inc. Due to The firm received complaints for...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VER2 HANDLE Recalled by Zimmer, Inc. Due to The firm received complaints for...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 23.5 Deg Rasp Handle Assy- LEFT Nonsterile Recalled by Zimmer, Inc. Due to...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VER2 DBL OFFSET RASP HANDLE Recalled by Zimmer, Inc. Due to The firm...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VI DBL OFFST W/ LRG STPL Recalled by Zimmer, Inc. Due to The firm received...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 23.5 Deg Rasp Handle Assy- RIGHT Nonsterile Recalled by Zimmer, Inc. Due to...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vl DBL OFFST WI LRG STPL Recalled by Zimmer, Inc. Due to The firm received...
The Issue: The firm received complaints for failure of the handle to remain assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 0.9 Sodium Chloride Injection Recalled...
The Issue: BD received some reports of open seals found on the BD Posiflush SF Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.