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. 2,580 recalls have been distributed to Nebraska in the last 12 months.
Showing 12421–12440 of 49,150 recalls
Recalled Item: TEG 5000 Functional Fibrinogen Reagent Recalled by Haemonetics Corporation...
The Issue: Due to a shift in the citrated blood range for a normal population, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4 Series CX phototherapy units equipped with Daavlin's ClearLink Control...
The Issue: Software issue, resuming an interrupted treatment will result in swap of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Field replacement back up batteries distributed on or after April 1 Recalled...
The Issue: Backup batteries can fail earlier than their estimated life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Back up batteries in Avance CS2 and Avance CS2 Pro Recalled by GE...
The Issue: Backup batteries can fail earlier than their estimated life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioTek EP-TRACER Software V2.x. Recalled by CardioTek BV Due to Device...
The Issue: Device did not pass electrical safety testing for adequate insulation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zonisamide Capsules USP Recalled by Glenmark Pharmaceuticals Inc., USA Due...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zonisamide Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin HCl 1.5 g in 0.9% Sodium Chloride Recalled by SCA Pharmaceuticals...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norepinephrine 8mg in 0.9% Sodium Chloride 250 mL bag Recalled by SCA...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zonisamide Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl 2mcg/ml and Bupivacaine 0.125% in 0.9% Sodium Chloride 100 mL bags...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Accupril (Quinapril HCl Tablets) 20 mg Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Accupril (Quinapril HCl Tablets) 10 mg Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Accupril (Quinapril HCl Tablets) 40 mg Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Start-up time for the flow rate range greater than 50 ml/hr, and less than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II Gastrointestinal Videoscope-indicated for use within the upper...
The Issue: Part (A-rubber) intended for a different model of gastrointestinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Peripheral Vascular Inc Due to There is the potential that...
The Issue: There is the potential that a 6 Fr Catheter Drainage kit contains an 8 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonovideoscope Model CF-H180AL Recalled by Olympus Corporation of the...
The Issue: A (Camera unit) CCD intended for a different model of colonoscope may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 Recalled by Smith &...
The Issue: Right nails were anodized, marked, and labelled as left nails and vice versa
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivenix Infusion System (IIS) Recalled by Ivenix, Inc. Due to Downstream...
The Issue: Downstream occlusion alarm is sometimes immediately followed by a pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.