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. 2,498 recalls have been distributed to Kentucky in the last 12 months.
Showing 19001–19020 of 28,748 recalls
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-120: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-112: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-112: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-120: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-115BT: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-112BT: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-115: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-120BT: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-130: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-115: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-110: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Cisco 3850 layer 3 switch Recalled by Philips Electronics North...
The Issue: May experience a loss of centralized monitoring.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo EZ Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Juno DRF Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX Endovascular AAA System Recalled by Endologix Due to Endologix updated...
The Issue: Endologix updated the Instructions for Use (IFU) and implemented...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX Endovascular AAA System Recalled by Endologix Due to Endologix updated...
The Issue: Endologix updated the Instructions for Use (IFU) and implemented...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cryptococcal Antigen Lateral Flow Assay (CrAg LFA) Recalled by...
The Issue: The affected products have approximately a 91% specificity while the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo DRF Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.