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. 1,976 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,976 in last 12 months

Showing 1262112640 of 28,748 recalls

Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion-Suture Trays SUT10140 SUTURE TRAY SUT10290 LACERATION TRAY...

The Issue: Incomplete seals on the sterile package may compromise the sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Aviva Plus Retail Strips 50 ct - intended for Recalled by Roche...

The Issue: Inability to dose the test strips, may result in a temporary inability to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion-General Surgery Convenience Kits DYNDH1033B SUBCLAVIAN ON/OFF KIT...

The Issue: Incomplete seals on the sterile package may compromise the sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion-Suture Tray DYNDR1210A SUTURING TRAY Recalled by Centurion Medical...

The Issue: Incomplete seals on the sterile package may compromise the sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion-BIOPSY TRAY BT205A MINOR SET UP BIOPSY TRAY BT345A HH PACK BIOPSY...

The Issue: Incomplete seals on the sterile package may compromise the sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion- I86625 DEBRIDEMENT TRAY Recalled by Centurion Medical Products...

The Issue: Incomplete seals on the sterile package may compromise the sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion- PT225 PAIN MANAGEMENT TRAY Recalled by Centurion Medical Products...

The Issue: Incomplete seals on the sterile package may compromise the sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion Chest Tube Trays: Kit Code Product CHT1170 CHEST TUBE Recalled by...

The Issue: Incomplete seals on the sterile package may compromise the sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion- HT5555A HYPERALIMENTATION & DRSG CHG TRAY Recalled by Centurion...

The Issue: Incomplete seals on the sterile package may compromise the sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2019· bioMerieux, Inc.

Recalled Item: VIDAS Varicella Zoster IgG (VZG) antibody IVD Recalled by bioMerieux, Inc....

The Issue: Two batches of VIDAS Varicella-Zoster IgG (VZG ) may yield an invalid...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2019· Abbott Medical

Recalled Item: Fast-Cath Hemostasis Introducer Recalled by Abbott Medical Due to Three lots...

The Issue: Three lots of Fast-Cath Hemostasis Introducer devices contained 8F sized...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2019· Abbott Medical

Recalled Item: Fast-Cath Trio HEMOSTASIS INTRODUCER Recalled by Abbott Medical Due to...

The Issue: Fast-Cath Trio Hemostasis Introducer devices contained 12F sized dilators...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2019· Karl Storz Endoscopy

Recalled Item: Karl Storz SE & Co. KG Recalled by Karl Storz Endoscopy Due to The firm has...

The Issue: The firm has become aware that there is a potential that the glass cover at...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2019· Medtronic Navigation, Inc.

Recalled Item: Mazor X Surgical System Positioner Type II Recalled by Medtronic Navigation,...

The Issue: There is a potential for the surgical system to detach from the operational...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2019· Stryker GmbH

Recalled Item: Stryker T2 Alpha Delta Strike Plate IMN Instruments - part Recalled by...

The Issue: Instrument can break at the level of the thread when being exposed to high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· Johnson & Johnson Surgical Vision Inc

Recalled Item: Healon GV PRO 0.85 mL Recalled by Johnson & Johnson Surgical Vision Inc Due...

The Issue: Ophthalmic viscosurgical device may be difficult to remove from the eye,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v17) bone densitometer...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA Advance (iDXA with enCORE v16) bone densitometer Recalled by GE...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v18) bone densitometer...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA bone densitometer Recalled by GE Healthcare, LLC Due to An issue...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing