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. 933 recalls have been distributed to Nebraska in the last 12 months.
Showing 44201–44220 of 49,150 recalls
Recalled Item: Synthes Soft Tissue Retractor Small Extendible. Offset blade facilitates...
The Issue: The small extendible Soft Tissue Retractor was recalled due to locking nut...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Raw Pistachio Halves Recalled by Superior Nut Co. Inc. Due to Potential...
The Issue: Positive laboratory result for Salmonella sp. Speciation in progress.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Breaded Recalled by Gourmet Express Marketing, Inc. Due to Packages of...
The Issue: Packages of breaded shrimp failed to declare shellfish (shrimp) and wheat...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "***Flo Trac Sensor Model MHD85***" Sterile Recalled by Edwards...
The Issue: The Edwards Lifesciences FloTrac Sensor is being recalled due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Matrix Threaded Persuader Deformity is a comprehensive thoracolumbar...
The Issue: Synthes became aware that during a procedure using the Matrix Threaded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujinon/Fujifilm Ultrasonic Endoscope Intended to provide ultrasonic images...
The Issue: A limited number of endoscopes were shipped to FMSU-ESD with a manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Tensioning Device The Synthes Osteogenesis System Recalled by...
The Issue: All lots of the Synthes Tensioning Device were recalled due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slipped Capital Femoral Epiphysis System Product Usage: Intended for...
The Issue: There is a possibility for the Guide Wires of the Slipped Capital Femoral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4 and 2.7 MM Locking Screw SLF-TPNG with T8 Stardrive Recalled by Synthes...
The Issue: Specific lots of the SS 2.4mm and SS 2.7mm Locking Screw (self-tapping) due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BuPROPion Hydrochloride Extended-Release Tablets (XL) Recalled by Actavis...
The Issue: Failed Dissolution Specifications: Dissolution test results at 8 hour...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Belladonna Alkaloids with Phenobarbital Tablets Recalled by West-Ward...
The Issue: Presence of Foreign Substance: black specks comprised of degraded organic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets Recalled by West-Ward Pharmaceutical Corp. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Synergetics 25 gauge Soft Tip Cannula Recalled by Synergetics Inc Due to One...
The Issue: One lot of 25 gauge Soft-Tip Disposable Cannulas are co-mingled with 23...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.