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. 931 recalls have been distributed to Kentucky in the last 12 months.
Showing 47621–47640 of 51,386 recalls
Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Long Recalled...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System (product code 6802783) Product Usage:...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versaport Bladeless Optical Fixation Cannula - 5mm Short Product Code:...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leucadia Autolok" Polyaxial Pedicle Screw System. Intended to help provide...
The Issue: Alphatec Spine initiated this medical device recall for the following...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versaport Bladeless Optical Trocar With (2) Fixation Cannulae - 5mm Recalled...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anspach MIA 16 (16cm Minimally Invasive Attachment) Recalled by The Anspach...
The Issue: Product did not reach expected sterility assurance level
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHO¿ Assay Software (OAS) Server Recalled by Ortho-Clinical Diagnostics...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System (product code 6802413) Product Usage: For...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension(R) Chemistry Wash (RD701) Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics received complaints of Chemistry Wash causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Short...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadSuite software. The firm name on the label is Merge Healthcare Recalled...
The Issue: Multiple studies were missing at a customer location that never made it to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large Tear Cross Cut Rasp 14mm x 7mm Ref. 5100-37-114 Recalled by Surgical...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: -Scorpion Needle Recalled by Surgical Instrument Service And Savings, Inc....
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: -Instratek Carpal Tunnel Release Blades Recalled by Surgical Instrument...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - Calf Garment Standard Ref. L501-M Lot 122549 Recalled by Surgical...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - IDEAL 30 Suture Grasper (Green) 30 Degree Ref. 251721 Recalled by Surgical...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - Re-New II Endocut Scissor Tip Recalled by Surgical Instrument Service And...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: -90 Degree L-Hook Tip Arthroscopic Electrode Recalled by Surgical Instrument...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - ACCU-PASS Suture Shuttle Recalled by Surgical Instrument Service And...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - ENDOPATH Resposable Bladeless Trocar Recalled by Surgical Instrument...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.