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. 1,831 recalls have been distributed to Kansas in the last 12 months.
Showing 27621–27640 of 28,538 recalls
Recalled Item: 100 ft roll of tubing inside a cardboard box. Medical Recalled by Steris...
The Issue: On 7/20/2012 the firm became aware that a lot of tubing was distributed by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E-Z WIDER BARIATRIC CHAIR BED Recalled by Kreg Medical Inc. Due to An EZ...
The Issue: An EZ Wider bed (capacity of 1000 lb. safe working load collapsed during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 220amx 30kw Mobile X-ray System The Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DGPHP RFA High-Power Single Use Grounding Pads and Cool-Tip RFA Recalled by...
The Issue: Covidien is conducting a recall of various production lots of DGHP RFA High...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 220amx 15kw Mobile X-Ray System The Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 200 amx with Digital Upgrade. The Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The SYSTEM 1E Liquid Sterilant Processing System. The SYSTEM 1E Recalled by...
The Issue: The firm initiated a recall after complaint investigations revealed that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V60 Ventilator Recalled by Respironics California Inc Due to Respironics is...
The Issue: Respironics is recalling the V60 ventilator because certain blower motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Custom Implant Devices Packaging: Packaging was not standardized on...
The Issue: In connection with a Warning Letter received from the U.S. Food & Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEXIS Imaging Suite - catalog number 1.008.7932 Recalled by Imaging Sciences...
The Issue: A condition can occur during renumbering of the patient database using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emit(R) 2000 Phenobarbital Assay (OSR4D229) and Syva(R) Emit(R)...
The Issue: Firm has confirmed highter imprecision with the recalled lots on Beckman...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The MAYFIELD¿ Horseshoe Gel Pads are used in conjunction with Recalled by...
The Issue: An investigation of customer complaints identified that for two product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Bio-Rad MONOLISA Anti-HBs EIA is for In Vitro Diagnostic Recalled by...
The Issue: Prolonged exposure of the MONOLISA Anti-HBs EIA Conjugate Diluent component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multileaf Collimator To be used for single or multiple fractions Recalled by...
The Issue: Information released with the product Agility did not originally contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX Cardiovascular (CV) Reporting Reporting tool used for structured...
The Issue: Content entered into the "Conclusions" free text box on the Report Writer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TxRx Knee 15 Coil 3T. For use in conjunction with Recalled by Quality...
The Issue: On July 27, 2012, it was reported to the firm that the Siemens 3T 15ch Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The MAYFIELD¿ Horseshoe Gel Pads are used in conjunction with Recalled by...
The Issue: An investigation of customer complaints identified that for two product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System 1 base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...
The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart FRx 861304 Automated External Defibrillator Manufactured...
The Issue: Philips determined that it is important to clarify information in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips and Laerdal brands of HeartStart HS1 Defibrillator Family Model...
The Issue: Philips determined that it is important to clarify information in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.