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. 2,646 recalls have been distributed to Kentucky in the last 12 months.
Showing 5861–5880 of 28,748 recalls
Recalled Item: RayCare software Recalled by RAYSEARCH LABORATORIES AB Due to An issue was...
The Issue: An issue was found in Software RayCare 5A, 5B, 6A, including service packs,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Aneurysm Clip TITANIUM Paddle-Clip Recalled by Peter Lazic Gmbh Due to...
The Issue: Wrong product coloring. The paddle clips should be blank, but they are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Aneurysm Clip TITANIUM Paddle-Clip Recalled by Peter Lazic Gmbh Due to...
The Issue: Wrong product coloring. The paddle clips should be blank, but they are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Embrace2- Indicated for use as an adjunct to seizure monitoring Recalled by...
The Issue: May have a battery life lasting less than the full 48 hours, requiring the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP Family 50 Series Models as follows: In vitro Recalled by...
The Issue: Sample misidentification could occur under specific conditions and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Redwood 2.0 ultrasound systems Recalled by Siemens Medical Solutions...
The Issue: If a user-generated preset for an 18L6 transducer created on a 1.0...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to Lipemic interference...
The Issue: Lipemic interference failed to meet the performance specification listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Air/Water Valve is provided/used with the following Endoscopes:...
The Issue: The air/water valve MAJ-1444 used with OER-Pro and OER-Elite may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX S Recalled by Medicrea International Due to There is a potential for a...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX C+ Recalled by Medicrea International Due to There is a potential for...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX MANTA Recalled by Medicrea International Due to There is a potential...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carina Sub-Acute Care Ventilator Recalled by Draeger Medical, Inc. Due to...
The Issue: Presence of polyether polyurethane (PE-PUR) and emission of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX ALIF Recalled by Medicrea International Due to There is a potential...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GRANVIA-C Recalled by Medicrea International Due to There is a potential for...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX MANTA+ Recalled by Medicrea International Due to There is a potential...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX DLIF Recalled by Medicrea International Due to There is a potential...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX 3D Recalled by Medicrea International Due to There is a potential for...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX TLIF Recalled by Medicrea International Due to There is a potential...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PASS LP Recalled by Medicrea International Due to There is a potential for a...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX ALIF S/A Recalled by Medicrea International Due to There is a...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.