Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,383 recalls have been distributed to Wyoming in the last 12 months.
Showing 24121–24140 of 27,462 recalls
Recalled Item: CODMAN CERTAS Programmable Valves Recalled by Codman & Shurtleff, Inc. Due...
The Issue: Ensuring all customers have the tools to assist in verifying the setting of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System Recalled by Terumo...
The Issue: Sterility of medical devices intended for use in surgical procedures may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stand-Alone Resuscitation Recalled by GE Healthcare Due to Medical device...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is Recalled...
The Issue: On December 13, 2012, King Systems initiated a voluntary recall of one (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panda iRes¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upgrade Kit Recalled by GE Healthcare Due to Medical device adjustment knob...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential safety issue involving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External Implant RBT Recalled by BioHorizons Implant Systems Inc Due to The...
The Issue: The body length of the External Implant 40105D3 Lot 1302762 labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator with CO2/EtCO2 Measurement The...
The Issue: MRx defibrillator displays a -?- for EtCO2 and does not display EtCO2 values...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gambro Cartridge Blood Set Recalled by Gambro Renal Products, Incorporated...
The Issue: Occluded heparin tubing events preventing anticoagulation dosing on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 29ga Oshima Dual Chandelier Recalled by Synergetics Inc Due to Faulty seals...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wide Field Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stiff 25ga Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 27ga ONE-STEP (tm) Awh/Tano Vivid Chandelier Recalled by Synergetics Inc Due...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrocare SPORTS MEDICINE Recalled by ArthroCare Medical Corporation Due to...
The Issue: A sharp edge on the cannulated tip of the device may damage or cut a suture.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 23ga Wide Field Endo Illuminator Recalled by Synergetics Inc Due to Faulty...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.