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. 1,049 recalls have been distributed to Kentucky in the last 12 months.
Showing 17441–17460 of 51,386 recalls
Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4 Recalled by RAYSEARCH LABORATORIES AB Due to Two issues were...
The Issue: Two issues were found with the treatment plan report: 1) There may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Capiox FX25 (West) Advance Oxygenator- with left port Recalled by Terumo...
The Issue: Capiox FX25 Advance oxygenator may be the incorrect configuration (East vs....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI 380 Electrocardiograph - Product Usage: intended to be a...
The Issue: The radio within the device can become disassociated with the wireless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (Adult Elongated O2/CO2 Mask - Product Usage: intended Recalled by Westmed,...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Elongated CO2/O2 Mask Recalled by Westmed, Inc. Due to There is a...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Procedure Kit Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Angiography/Angioplasty custom kits contain header bags which may not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoPatch SG Pulmonary Human Cardiac Patch. The patch is cryopreserved...
The Issue: On November 10, 2020, it was discovered that there are post- processing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROKERA Plus Recalled by TissueTech, Inc. Due to Potential exposure of...
The Issue: Potential exposure of product to microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoValve SG Pulmonary Human Heart Valve. The valve is cryopreserved...
The Issue: On November 10, 2020, it was discovered that there are post- processing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROKERA Recalled by TissueTech, Inc. Due to Potential exposure of product to...
The Issue: Potential exposure of product to microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROKERA Slim Recalled by TissueTech, Inc. Due to Potential exposure of...
The Issue: Potential exposure of product to microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniCap Extended Life PD Transfer Set Recalled by Baxter Healthcare...
The Issue: Potential for no-flow and leaks under the twist clamp.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Code: K12T-02871 Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Angiography/Angioplasty custom kits contain header bags which may not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter Recalled by Applied...
The Issue: The products subject to this recall may contain obvious, incorrect pouch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Code: K05T-02533 Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Angiography/Angioplasty custom kits contain header bags which may not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levetiracetam Tablets Recalled by EYWA PHARMA INC Due to Presence of foreign...
The Issue: Presence of foreign tablet/capsule: A 1000 mg Levetiracetam Tablet was found...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shimadzu Mobile X-Ray System Recalled by Shimadzu Medical Systems Due to...
The Issue: There is a potential that the adjustable handle option on the X-Ray system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.