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. 1,073 recalls have been distributed to Kentucky in the last 12 months.
Showing 13181–13200 of 28,748 recalls
Recalled Item: LEEP Return Patient Pads (10/ box) Model # 6050Pl used Recalled by...
The Issue: Discrepancy between the correct expiration dates on the individual pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 RIGHT Catalog Recalled by...
The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. 01-1503-0032 (Adolescent Nail Attachment Bolt). Component of the...
The Issue: Binding can occur between the attachment bolt and intramedullary nail, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 LEFTTriathlon Femoral...
The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 RIGHT Catalog Recalled by...
The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoPediatrics Adolescent attachment bolt used with the Pediatric Nailing...
The Issue: Interference can occur between the adolescent attachment bolt and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 LEFT Catalog Recalled by...
The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the...
The Issue: Binding can occur between the attachment bolt and intramedullary nail, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci SP Camera Recalled by Intuitive Surgical, Inc. Due to Some cameras...
The Issue: Some cameras were found to have residual soil adhered to the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RespVent Closed Suction System T-Piece Tracheostomy Adult Recalled by...
The Issue: It has been determined that some units of catheters were not tightly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irrisept Wound Debridement and Cleansing System. 12 units per case. Recalled...
The Issue: Potential defect in the sterile pouch seal, which may result in a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 59 mm Item # 195750 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-CR Tibial Tray - Interlok 63mm Item # 195269 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard XP Tibial Tray 69 mm Item # 195248 Recalled by Zimmer Biomet, Inc....
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 75 mm Item # 195757 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 67 mm Item # 195753 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-CR Tibial Tray - Interlok 71mm Item # 195273 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-CR Tibial Tray - Interlok 83 mm Item # 195277 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard XP Tibial Tray 67 mm Item # 195247 Recalled by Zimmer Biomet, Inc....
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard XP Tibial Tray 79 mm Item # 195252 Recalled by Zimmer Biomet, Inc....
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.