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 1256112580 of 28,748 recalls

Medical DeviceDecember 16, 2019· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...

The Issue: Centricity Universal Viewer measurements saved into a DICOM Grayscale...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Nextremity Solutions

Recalled Item: Stratum Lapidus Plate - Small Rt Recalled by Nextremity Solutions Due to The...

The Issue: The product contains a different plate than indicated by the package...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 24MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Corrugated Humidification System with Remote...

The Issue: There is the potential for water to flood the column and enter the circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· CooperSurgical, Inc.

Recalled Item: ADVANCED ENDOSEE System CANNULA Recalled by CooperSurgical, Inc. Due to...

The Issue: Potential for unsealed pouches in two (2) lots of the Endosee Advance...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Corrugated Humidification System Recalled by TELEFLEX...

The Issue: There is the potential for water to flood the column and enter the circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· Beckman Coulter Inc.

Recalled Item: Beckman Coulter MicroScan PROMPT Inoculation System-D Recalled by Beckman...

The Issue: Due to customer reports it has been determined that the inoculation system...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Humidification System With Remote Temperature Port...

The Issue: There is the potential for water to flood the column and enter the circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Humidification System Recalled by TELEFLEX MEDICAL...

The Issue: There is the potential for water to flood the column and enter the circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 12, 2019· Baxter Healthcare Corporation

Recalled Item: ONE-LINK Needle-free IV Connector Recalled by Baxter Healthcare Corporation...

The Issue: Continu-Flo sets with male Luer bodies at the lower end of, and within, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2019· Baxter Healthcare Corporation

Recalled Item: Clearlink System Continu-Flo Administration Sets Recalled by Baxter...

The Issue: Continu-Flo sets with male Luer bodies at the lower end of, and within, the...

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- P151659 BIOPSY TRAY P243133 LATEX TUBING PACK P243133 LATEX...

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-Surgical trays DYNJ04079Z CIRCUMCISION TRAY STERILE DYNJ08835...

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- Laceration Trays DYNDL1073 LACERATION TRAY DYNDL1152A LACERATION...

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 Dental Kits DH775 PREMIUM DENTAL EXAM TRAY DYKA1169B DENTAL...

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-Vaginal Speculum VS2000LST STERILE ER VAGINAL SPECULUM W/LIGHT...

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-Trays EBSI1021 VALVE CHANGE KIT- DOUBLE 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 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion PICC : CVI2650 ANGIO TRAY CVI3610 CENTRAL LINE INSERTION Recalled...

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-LVAD Kits DM1005 DAILY LVAD MAINTENANCE KIT DM280A LVAD MANAGEMENT...

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- Dressing Tray M101156A DRESSING TRAY M101167A DRESSING 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