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 26361–26380 of 28,748 recalls
Recalled Item: Pinnacle¿ Destination¿ Peripheral Guiding Sheath Recalled by Terumo Medical...
The Issue: Medical devices were incorrectly labeled with extended expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TotalCare Bed used with AccuMax Quantum VPC mattress AccuMax Quantum...
The Issue: When the bed is put into the chair egress position, the magnets on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEO-MED ORTHO TOTAL JOINT TRACECART(R) Recalled by DeRoyal Industries Inc...
The Issue: DeRoyal recalled kits that contained Stryker togas which were recalled for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Glidesheath (tm) Recalled by Terumo Medical Corporation Due to...
The Issue: Medical devices were incorrectly labeled with extended expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******QTY 1***APEX Arthroscopy Tubing Set. Intended for use for Recalled by...
The Issue: Conmed Linvatec received complaints that their products C7120 APEX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3 (TM) XLPE ACETABULAR LINER UHMWPE Recalled by Smith & Nephew Inc Due to...
The Issue: One batch of 60 mm 20o R3 XLPE liner may be laser etched and packaged as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens MEVATRON series Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: The information regarding the FILM Mode calibration may have been considered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3 (TM) XLPE ACETABULAR LINER UHMWPE Recalled by Smith & Nephew Inc Due to...
The Issue: One batch of 60 mm 20o R3 XLPE liner may be laser etched and packaged as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR S4 with Variable Spot Scanning Excimer System (STAR S4) Recalled by...
The Issue: Under specific conditions, there is an unlikely potential to result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VenaFlow Elite 30B-B and 30BI-B Product Usage: The VenaFlow Elite Recalled...
The Issue: DJO, LLC has recently identified a product safety issue with the battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNCHRON System(s) Lactate (LACT) Reagent. Product Usage: Lactate (LACT)...
The Issue: Beckman Coulter has confirmed customer reports of LACT Lot M210077 failing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StarDental Classique(TM) Diamond Dental Bur. Used for specific applications...
The Issue: Recall was initiated because a manufacturing issue was found that prevented...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR S4 IR Excimer System (STAR S4 IR) Mfg by AMO Manufacturing USA Recalled...
The Issue: Under specific conditions, there is an unlikely potential to result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.