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. 982 recalls have been distributed to Nebraska in the last 12 months.
Showing 36201–36220 of 49,150 recalls
Recalled Item: Stryker UniVise Spinous Process Fixation Plate System Inserter Recalled by...
The Issue: The Inserter Inner Shaft would not fit through the Inserter. The inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prism Medical P-300 Portable Consumer Lift Recalled by ErgoSafe Products,...
The Issue: Drive shaft and over speed arm may simultaneously fail potentially resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prism Medical C-300 Consumer Ceiling Lift Recalled by ErgoSafe Products, LLC...
The Issue: Drive shaft and over speed arm may simultaneously fail potentially resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specialist 2 Intramedullary (SP2 IM) Rod 400mm Instrument (PN 96-6120)...
The Issue: DePuy Orthopaedics, Inc. is initiating a voluntary recall of select lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis...
The Issue: Complaints that the femoral head could not be assembled with its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnVision FLEX/HRP visualization reagent found in the following kits:...
The Issue: There is a defect in one lot of a buffer, non-specific background staining...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.0mm Unit Rod 270mm Recalled by Synthes (USA) Products LLC Due to This...
The Issue: This product was produced using a finishing process not identified as part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgicept (Ethyl alcohol 70% w/w) WATERLESS Surgical Hand Scrub & Recalled...
The Issue: Chemical Contamination: Naphthalene compound identified in the product after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenoglide (fenofibrate) tablets Recalled by Valeant Pharmaceuticals North...
The Issue: Failed Dissolution Specifications: Failed 24 month dissolution testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3-Day Cleanse Recalled by TN Juice Bar Due to Unpasteurized juice product...
The Issue: Unpasteurized juice product with elevated pH levels and unlabeled almond...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AMSCO 400 and AMSCO C Small Steam Sterilizers Recalled by Steris Corporation...
The Issue: In AMSCO Small Steam Sterilizers equipped with the CS-iQ feature, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novocastra Lyophilized Mouse Monoclonal Antibody CD10 (CD10)....
The Issue: These Lot numbers are not stable up to the expiry date on the product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail CM Long. Intramedullary Fixation Rod. The Zimmer...
The Issue: In about 5% of tested samples, the outer tray was found to be compromised....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH + LOMB Biotrue ONEday lenses (nesofilcon A) Recalled by Bausch & Lomb...
The Issue: The firm determined that 25 lots had been manufactured with a minor surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inserter for Titanium Elastic Nails (TEN) Recalled by Synthes (USA) Products...
The Issue: potential for mechanical failures such as breakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas b 123 POC system The cobas b 123 POC Recalled by Roche Diagnostics...
The Issue: under specific settings, an issue may occur during simultaneous Sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylcobalamin 20 mg/mL PF Injection Recalled by Kalman Health & Wellness,...
The Issue: Lack of Assurance of Sterility: A recall of all compounded sterile...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HCG 3000 Units/mL Injection Recalled by Kalman Health & Wellness, Inc. dba...
The Issue: Lack of Assurance of Sterility: A recall of all compounded sterile...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TRIMIX SPECIAL (30 mg-1 mg-10 mcg/mL) Injection Recalled by Kalman Health &...
The Issue: Lack of Assurance of Sterility: A recall of all compounded sterile...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 17-Alpha Hydroxyprogesterone 250 mg/mL in Sesame Oil Injection Recalled by...
The Issue: Lack of Assurance of Sterility: A recall of all compounded sterile...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.