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. 2,672 recalls have been distributed to Kentucky in the last 12 months.
Showing 2841–2860 of 28,748 recalls
Recalled Item: Merlin@home with the MerlinOnDemand capability Transmitter Merlin@home with...
The Issue: Due to heart transmitter not being able to upgrade to the current software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT...
The Issue: Disposable biopsy instruments were potentially manufactured missing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 PSA assay Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: The IMMULITE 2000 PSA assay for use on the IMMULITE 2000 and IMMULITE 2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Flex Extenders Recalled by Westmed, Inc. Due to Due to connector within...
The Issue: Due to connector within the circuit flex extender not meeting specifications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMBU / KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject U-100 1 mL Insulin Syringe Luer-Lock with Tip Cap Soft Pack...
The Issue: Certain lots of listed lots of Cardinal Health Monoject U-100 1 mL Insulin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: intelliPATH Universal HRP Detection Kit Recalled by Biocare Medical, LLC Due...
The Issue: Kits containing the DAB chromogen buffer, intended for use in either manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System Recalled...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed that a negative sodium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Vial2Bag Advanced¿ Product Name: Vial2Bag Advanced¿ 20mm...
The Issue: Due to packaging damage from heat exposure during shipping/transportation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS MALE-FEMALE MIDSECTION 40MM. Part Number: 25001040E. Component of...
The Issue: Potential challenge with intraoperative assembly of the external taper of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard KIT Recalled by AVID Medical, Inc. Due to Foreign Object Contamination
The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard PACEMAKER PACK - Medical convenience kits Model Number: MAMC223-08...
The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard KIT Recalled by AVID Medical, Inc. Due to Foreign Object Contamination
The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.