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. 2,634 recalls have been distributed to Kentucky in the last 12 months.
Showing 8821–8840 of 28,748 recalls
Recalled Item: Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Recalled by...
The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Recalled by...
The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare AVIVA Storm RX with LiNX Gyro Power Wheelchair (with Recalled by...
The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruDi NAV Suction Instruments: 0-Degree Recalled by Acclarent, Inc. Due to...
The Issue: Suction Instruments were incorrectly calibrated so they may not meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BV Endura with Software Release 2.3- A mobile Recalled by Philips North...
The Issue: Instructions for Use do not specify the maximum surface temperature of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veradius Unity with Software Release 2.1- Amobile Recalled by Philips North...
The Issue: Instructions for Use do not specify the maximum surface temperature of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BV Pulsera with Software Release 2.3-A mobile Recalled by Philips North...
The Issue: Instructions for Use do not specify the maximum surface temperature of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stealthstation System w/ Stealthstation Cranial Software 3.1.1 Recalled by...
The Issue: Cranial biopsy procedure software can enter a state where the biopsy depth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O3D ORCHESTRATE Orthodontic Technologies User Manual and Data Processing...
The Issue: Due to product label/labeling being altered from it's approved state.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIVO Blood Collection Device 20G Recalled by Velano Vascular Due to...
The Issue: Incomplete sealing of blood collection device unit packages may produce a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iontoPATCH On-the-Go Patch Therapy Recalled by Tapemark Company Due to The...
The Issue: The dosage information on the pouch is incorrect; the primary carton label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNCHRON Systems Cholesterol (CHOL) Reagent Recalled by Beckman Coulter Inc....
The Issue: Cholesterol Reagent may fail with Out of Calibration Range Low (OCR Low)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPID 20 E Recalled by Biomerieux Inc Due to There is an error in the new...
The Issue: There is an error in the new version of the package insert. The Reading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torosa Saline-Filled Testicular Prosthesis (Size Small) Recalled by...
The Issue: Product is mislabeled for size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stealth Autoguide Tracker Recalled by Medtronic Navigation, Inc. Due to A...
The Issue: A tracker that holds and guides neurosurgical surgical instruments may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Miami J Select Collar Recalled by Ossur Americas Due to Instructions for use...
The Issue: Instructions for use were updated to include additional information to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel (US IVD under FDA EUA 200075)...
The Issue: The firm identified sixteen (16) faulty cartridges in LOT 210209, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific ROTAPRO Recalled by Boston Scientific Corporation Due to...
The Issue: Manufacturing instructions did not include the directions to not retest the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigniCap Delta Scalp Cooling System Recalled by Dignitana, Inc. Due to...
The Issue: Instructions for Use (IFUs) updated to include use of a headband is now...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...
The Issue: The firm identified that the Vscan Extend device will not power on because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.