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. 2,469 recalls have been distributed to Kentucky in the last 12 months.
Showing 24101–24120 of 28,748 recalls
Recalled Item: Tibila Insert UC Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Foley Urinary Catheter Insertion Tray with 10cc syringe Recalled by...
The Issue: Labeling error: The manufacturing date is the same as the expiration date....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table with Dual 2 Way Drop Section...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QLAB 10 Core Module PN 453561704771. QLAB Quantification Software is...
The Issue: The QLAB a2DQ and aCMQ features have a defect that may use incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emerald Fiberoptic Blade Recalled by Teleflex Medical Due to Packaging...
The Issue: Packaging Error: Customers have reported receiving incorrect product. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene BC-GN Test Kit (Catalog number 20-005-021) includes: 1) 20 Recalled...
The Issue: Nanosphere Inc. has recently determined through four customer complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QLAB 10.1 Core Module PN 453561728001. QLAB Quantification Software is...
The Issue: The QLAB a2DQ and aCMQ features have a defect that may use incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Recalled by Teleflex Medical Due to The temperature probe does...
The Issue: The temperature probe does not properly connect to the temperature port.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Hulka Clip is a sterile packaged medical device that Recalled by Richard...
The Issue: Richard Wolf Medical Instrument Corporation is recalling Hulka Clip Tubal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kodak DirectView DR 7500 Diagnostic X-Ray System Product Usage: The Recalled...
The Issue: An on-site evaluation of the equipment parts that attach the Beta Assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Recalled by Teleflex Medical Due to The temperature probe does...
The Issue: The temperature probe does not properly connect to the temperature port.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gyrus ACMI Falope-Ring Dilator Recalled by Gyrus Medical, Inc Due to...
The Issue: Falope-Ring Dilator for Reusable Falope-Ring Band Applicators have been sold...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Luminos dRF Recalled by Siemens Medical Solutions USA, Inc Due to It...
The Issue: It was discovered that during a RAD examination using Siemens Luminos dRF,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4001S Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4052 Endo Tube Holder Recalled by Smiths Medical ASD, Inc. Due to The tube...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System --- For use in the in vitro quantitative...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.