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. 2,555 recalls have been distributed to Kentucky in the last 12 months.
Showing 16741–16760 of 28,748 recalls
Recalled Item: SOMATOM Spirit(Model 10045692 ) Recalled by Siemens Medical Solutions USA,...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Perspective 16 (Model 10891666) Recalled by Siemens Medical...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Perspective (Model 10495568) Recalled by Siemens Medical Solutions...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Pneumatic Lithotripter Recalled by Cook Inc. Due to The...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Exhaust Cap Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Exhaust Line Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker C02 Cartridge Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Single Use Probe Recalled by Cook Inc. Due to The interior of...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Sterilization Cap Recalled by Cook Inc. Due to The interior of...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Probe Cap Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Calcium Flex¿ reagent cartridge Recalled by Siemens...
The Issue: May produce erroneously low results from specific well sets.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee...
The Issue: Customers may receive the incorrect size implant from what is labeled on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AltiVate Reverse INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: Broken or missing screws and retaining clips. This may be due to screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS CL Flow Cytometer System Recalled by Beckman Coulter Inc. Due to The...
The Issue: The device may process the same sample with two different sample IDs and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack: 1) UDI-M535SAK3010 Recalled by NxStage Medical, Inc....
The Issue: May contain endotoxin levels which have been confirmed to exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.