Product Recalls in Kansas
Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,090 recalls have been distributed to Kansas in the last 12 months.
Showing 7981–8000 of 28,538 recalls
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: NaturaLyte 2301 2K 3.0 Ca 1 Mg Gal Recalled by Fresenius Medical Care...
The Issue: The product was potentially exposed to below-recommended storage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: Philips Laser System Recalled by Spectranetics Corporation Due to The...
The Issue: The LAS-100 Laser system may detect an inoperable hardware component during...
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: 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: 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: 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: 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: a. SPS MEDICAL SUPPLY Steam Indicator Strip SPSmedical Sterilization...
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. Skin Adhesive McKesson LiquiBand Exceed 0.4 mL Liquid Dome 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: Cooper Surgical PREFILTER 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: a. STERIS CORP Celerity Celerity 20 Sterilization Indicator Challenge Pack...
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. Comply INDICATOR Recalled by Mckesson Medical-Surgical Inc. Corporate...
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: Medical Monofilament Manufacturing MONOFILIMENT TEST 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.
Recalled Item: 3M SYSTAGENIX/KCI KerraCel Ag DRESSING Recalled by Mckesson Medical-Surgical...
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: FISHER SCIENTIFIC Aseptic Control¿ LUBRICATING JELLY PAP TEST 4OZ(12/PK)...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.