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. 2,656 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,656 in last 12 months

Showing 42414260 of 51,386 recalls

Medical DeviceOctober 3, 2024· DeRoyal Industries Inc

Recalled Item: DeRoyal CHILDREN'S LAPTRACEPACK Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· DeRoyal Industries Inc

Recalled Item: DeRoyal CHILDREN'S ORTHOPEDIC TRACEPACK Recalled by DeRoyal Industries Inc...

The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· DeRoyal Industries Inc

Recalled Item: DeRoyal CHILDREN'S GENERAL TRACEPACK Recalled by DeRoyal Industries Inc Due...

The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· GE Healthcare

Recalled Item: GE Healthcare Centricity Universal Viewer Zero Footprint Recalled by GE...

The Issue: GE HealthCare has become aware of an issue in Centricity Universal Viewer...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· DeRoyal Industries Inc

Recalled Item: DeRoyal C-SECTION TRACEPACK Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2024· Smith & Nephew Medical, Ltd.

Recalled Item: RENASYS EDGE The RENASYS¿ EDGE pump is indicated for patients Recalled by...

The Issue: Due to issues with battery depletion and inability to recharge if the...

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

Class II — Potential Health HazardOngoing
DrugOctober 1, 2024· ACCORD HEALTHCARE, INC.

Recalled Item: Cisplatin Injection Recalled by ACCORD HEALTHCARE, INC. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 1, 2024· Advanced Medical Solutions Ltd.

Recalled Item: MEDLINE MAXORB EXTRA ALGINATE WOUND DRESSING 4X4 SQUARE Recalled by Advanced...

The Issue: Due to defects on primary packaging pouch that compromise the device's...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2024· Advanced Medical Solutions Ltd.

Recalled Item: Hollister CalciCare Calcium Alginate Dressing calcium alginate dressings...

The Issue: Due to defects on primary packaging pouch that compromise the device's...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2024· Advanced Medical Solutions Ltd.

Recalled Item: McKesson Calcium Alginate Dressing MFR# 3562 Wound dressing indicated for...

The Issue: Due to defects on primary packaging pouch that compromise the device's...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2024· Abbott Medical

Recalled Item: Merlin@home Transmitter The Merlin@home" (M@h) transmitter is intended...

The Issue: Due to heart transmitter not being able to upgrade to the current software...

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

Class III — Low RiskOngoing
Medical DeviceOctober 1, 2024· Abbott Medical

Recalled Item: Merlin@home with the MerlinOnDemand capability Transmitter Merlin@home with...

The Issue: Due to heart transmitter not being able to upgrade to the current software...

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

Class III — Low RiskOngoing
DrugSeptember 30, 2024· Staska Pharmaceuticals, Inc.

Recalled Item: Ascorbic Acid Inj. Solution Recalled by Staska Pharmaceuticals, Inc. Due to...

The Issue: Presence of Particulate Matter: Presence of glass particulates.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 30, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Ciclopirox Gel 0.77% Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Defective Container: Firm received complaints of broken tube at the seal.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 30, 2024· Bard Peripheral Vascular Inc

Recalled Item: Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT...

The Issue: Disposable biopsy instruments were potentially manufactured missing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 PSA assay Recalled by Siemens Healthcare Diagnostics, Inc. Due...

The Issue: The IMMULITE 2000 PSA assay for use on the IMMULITE 2000 and IMMULITE 2000...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2024· Westmed, Inc.

Recalled Item: 1) Flex Extenders Recalled by Westmed, Inc. Due to Due to connector within...

The Issue: Due to connector within the circuit flex extender not meeting specifications...

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

Class II — Potential Health HazardOngoing
FoodSeptember 26, 2024· Walmart Inc

Recalled Item: Great Value Diced Peaches Recalled by Walmart Inc Due to FD&C Red No 3 was...

The Issue: FD&C Red No 3 was not declared as an ingredient.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund