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 11941–11960 of 49,150 recalls
Recalled Item: Ventana HE 600 System Recalled by Ventana Medical Systems Inc Due to There...
The Issue: There is a potential for fluid leak inside the Ventana HE 600 instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Aisys CS2 Anesthesia System Recalled by GE Healthcare, LLC Due...
The Issue: There is a potential reversal of the O2 and air cylinder pressure transducer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peak Universal Bond Self-Etch Bottle Kit Recalled by Ultradent Products,...
The Issue: SE primer may be missing some or all of the resin portion of the chemistry....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trader Joe's BBQ & Black Pepper Toscano Chopped Salad 11 oz. Contains Milk...
The Issue: Undeclared allergen (peanuts) from incorrect master pack. Salad kit contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...
The Issue: Software related alarm escalation defect occurs after approximately 25 days...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaviCare Nurse Call/Voalte Nurse Call Recalled by Baxter Healthcare...
The Issue: An issue has been identified with Phillips (Emergin) and Longleaf non relay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSSUR VARIFLEX SUBA JUNIOR foot and ankle external prosthesis Recalled by...
The Issue: Due to receiving complaints related to broken (cracked) prosthetic foot with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Avance CS2 Recalled by GE Healthcare, LLC Due to The base of...
The Issue: The base of the anesthesia system can have a crack and could potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLTIVE SuperPulsed Laser Fibers Recalled by Olympus Corporation of the...
The Issue: Device model and size for affected lots of Laser Fibers may be mismatched...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HammerTube Implant Recalled by Paragon 28, Inc. Due to Due to Titanium...
The Issue: Due to Titanium plasma coating not present implant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anti-SARS-CoV-2 IgG Quantitative Reagent Pack- Intended for use on VITROS¿...
The Issue: On-Analyzer Stability (OAS) time, supported for 6 weeks; not 8 weeks as is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rich s Milk Chocolate Giant Layered Peanut Butter and Cups Recalled by...
The Issue: Salmonella. Product made using recalled Jif peanut butter
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Artri King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ortiga mas Ajo Rey con Omega 3 Recalled by Amazon.com, Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artri Ajo King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due...
The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ethicon SURGIFLO Hemostatic Matrix Kit with Thrombin (6/CS) Recalled by...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE INDUSTRIES Medline Plug Recalled by Mckesson Medical-Surgical Inc....
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B. BRAUN MEDICAL INC. Anesthesia Support Tray SUPPORT TRAY Recalled by...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. MMS - IMMUNOSTICS INC McKesson Rapid Test Kit Consult Recalled by...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drugs of Abuse Tests: a. Wondfo Tdip Drugs of Abuse Recalled by Mckesson...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.