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. 2,497 recalls have been distributed to Kentucky in the last 12 months.
Showing 20081–20100 of 28,748 recalls
Recalled Item: Conserve Cups: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lineage Liners: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procotyl (Rim- Lock) Liners: Recalled by MicroPort Orthopedics Inc. Due to...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conserve Shells: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt Chromium Heads Transcend: 26000017 Recalled by MicroPort Orthopedics...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16 AW. Packed...
The Issue: The rear gradation scale was screen printed upside down on the flowmeter gauge.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PoleStar system (N20 / N30) Warning Lamps Control Box Recalled by Medtronic...
The Issue: Medtronic Navigation is recalling certain components of the PoleStar system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Image1 SPIES X-LINK Camera Control Unit (CCU) Recalled by Karl Storz...
The Issue: Potential electrical interference issue when the Image1 SPIES X-LINK and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ Chemistry (Syva Onboard) Theophylline_2 (THEO_2) Reagent is for in...
The Issue: Siemens Healthcare Diagnostics has confirmed the Syva¿ EMIT¿ 2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syva¿ EMIT¿ 2000 Theophylline - Catalog # 4P019UL /SMN#10445324 is Recalled...
The Issue: Siemens Healthcare Diagnostics has confirmed the Syva¿ EMIT¿ 2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achillon Minimally Invasive Device for Achilles Tendon Rupture Treatment The...
The Issue: Data from internal studies suggests there may be a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...
The Issue: This Pacing Lead System does not comply with Section 8.5.2.3 of IEC 60601-1,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB Sciex API 3200MD" LC/MS/MS System. In-Vitro Diagnostic Instrument Part...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX 3200MD QTRAP¿ LC/MS/MS System Mass Spectrometer for In-Vitro...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX Triple Quad 4500MD LC/MS/MS System. Mass Spectrometer for Recalled...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX QTRAP¿ 4500MD LC/MS/MS System Mass Spectrometer for In-Vitro...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith and Nephew TWINFIX QUICK-T Knot Pusher Suture Cutter Recalled by Smith...
The Issue: The device could be subject to breaches of its sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A7 Anesthesia Delivery System Recalled by Mindray DS USA, Inc. dba Mindray...
The Issue: Potential for a leak to occur on the back-up O2 and air e-size cylinder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spike Set Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T100-022WF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.