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. 1,736 recalls have been distributed to Nebraska in the last 12 months.
Showing 42941–42960 of 49,150 recalls
Recalled Item: Sandel Healthcare Safety Devices Weighted Safety Scalpel #3 Disposable...
The Issue: Select lots of SANDEL Weighted Safety Scalpels are packaged with the scalpel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Trabecular Metal Total Ankle Talar Component Right Sizes 1-6 Recalled...
The Issue: As part of routine manufacturing process monitoring by Zimmer, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Advanced Energy Aquamantys3 Pump Generator Recalled by Medtronic...
The Issue: The internal protection circuitry on the electrosurgical output that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 100NX Recalled by Advanced Sterilization Products Due to Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD NX Recalled by Advanced Sterilization Products Due to Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunrise Brand Zippie Voyage Recalled by Sunrise Medical (US) LLC Due to...
The Issue: There is a remote possibility for the plastic latch to deform over the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Assembly Recalled by Intuitive Surgical, Inc. Due to Reports of friction...
The Issue: Reports of friction within certain instrument arms can interrupt smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coulter LH 780 Hematology Analyzer Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is recalling the LH 750 and LH 780 Hematology Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Video Monitor Suspensions that may be on the following Fluoroscopic Recalled...
The Issue: Missing screws in the overhead Video Monitor Suspension. GE discovered that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZYM B Reagent () ZYM B reagent is an Recalled by Biomerieux France Chemin De...
The Issue: bioM¿rieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API Listeria () API Listeria is a standardized system Recalled by Biomerieux...
The Issue: bioM¿rieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliFill i.v. Pharmacy Compounding Device (PCD). Intended to fill...
The Issue: Following a retrospective review for Baxter Daytona Complaint CR-954, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coulter LH 750 Hematology Analyzer Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is recalling the LH 750 and LH 780 Hematology Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API NH () API NH is a standardized system Recalled by Biomerieux France...
The Issue: bioM¿rieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaSafe Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion...
The Issue: CareFusion is recalling the VersaSafe Extension Intravascular Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vega Sport Performance Protein Dietary Supplement Chocolate Powder....
The Issue: Sequel Naturals is recalling nine lots of products due to contamination by...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Plum Organics Sweet Potato Recalled by Plum Inc Due to Manufacturing defect...
The Issue: Manufacturing defect leading to post-process contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Plum Organics Blueberry Recalled by Plum Inc Due to Manufacturing defect...
The Issue: Manufacturing defect leading to post-process contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Plum Organics Apple & Carrot Organic Baby Food Recalled by Plum Inc Due to...
The Issue: Manufacturing defect leading to post-process contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Plum Organics Plum Recalled by Plum Inc Due to Manufacturing defect leading...
The Issue: Manufacturing defect leading to post-process contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.