Product Recalls in Kentucky
Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,457 recalls have been distributed to Kentucky in the last 12 months.
Showing 25241–25260 of 28,748 recalls
Recalled Item: Versys Build-Up Block The VerSys CRC Hip System is indicated Recalled by...
The Issue: Zimmer is initiating a lot specific recall of the CPT Hip Stem, Versys...
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: 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: Trabecular Metal (TM) Reverse Glenosphere 36mm Part 00-4349-036-11 The...
The Issue: Zimmer is initiating a lot specific recall of the CPT Hip Stem, Versys...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT Hip System Recalled by Zimmer, Inc. Due to Zimmer is initiating a lot...
The Issue: Zimmer is initiating a lot specific recall of the CPT Hip Stem, Versys...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC FX 40 instrument Recalled by Becton Dickinson & Co. Due to...
The Issue: Improperly functioning component of a diagnostic medical device may cause...
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: 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.
Recalled Item: BD BACTEC FX- Top Unit instrument Recalled by Becton Dickinson & Co. Due to...
The Issue: Improperly functioning component of a diagnostic medical device may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 23ga Wide Field Corona Endo Illuminator Recalled by Synergetics Inc Due to...
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: 25ga Wide Field Corona Endo Illuminator Recalled by Synergetics Inc Due to...
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: Standard tubing set Recalled by Synergetics Inc Due to Faulty seals on the...
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: PFC SIGMA Cruciate Retaining (CR) Recalled by DePuy Orthopaedics, Inc. Due...
The Issue: Knee implant femoral devices were found to have anomalous microstructure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 23ga Endo Illuminator (Eckardt Trocar Compatible) Recalled by Synergetics...
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: 25ga Awh Chandelier Recalled by Synergetics Inc Due to Faulty seals on the...
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: Vivid (tm) 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.