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 25221–25240 of 28,748 recalls
Recalled Item: Anspach Carbide Cutting Burrs: 1.5MMx7.5MM Cylindrical Carbide Drum part #...
The Issue: Some carbide cutting burr fractured during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 840 ventilator systems software part number 4-070212-85...
The Issue: Covidien is conducting a voluntary field corrective action on Puritan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 50 Sterilization System Recalled by Advanced Sterilization Products...
The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 100S Sterilization System Recalled by Advanced Sterilization...
The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD NX Sterilization System Recalled by Advanced Sterilization Products...
The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Artis zee Ceiling Systems. Angiographic x-ray system. Recalled by...
The Issue: During the lifetime of Artis zee Ceiling systems, there is an increased wear...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: SuperElastic Regular force NiTi lower or upper Natural arches. 0.14 Recalled...
The Issue: Labeling issue: Product labeled as "Upper" may contain "Lower" archwires...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SuperElastic Regular force NiTi lower or upper Natural arches. 0.16 Recalled...
The Issue: Labeling issue: Product labeled as "Upper" may contain "Lower" archwires...
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: 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: 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: 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: 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.