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. 2,672 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,672 in last 12 months

Showing 16811700 of 28,748 recalls

Medical DeviceMay 1, 2025· Straumann USA LLC

Recalled Item: GM Helix Acqua Implant Recalled by Straumann USA LLC Due to It is possible...

The Issue: It is possible that a package labelled as an 11.5 mm implant may contain a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2025· Beckman Coulter Mishima K.K.

Recalled Item: Sample probe sucks a sample dispensed into a tube or Recalled by Beckman...

The Issue: A manufacturing defect in the sample probe (S probe). The corners of the tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2025· Beckman Coulter Mishima K.K.

Recalled Item: Sample probe sucks a sample dispensed into a tube or Recalled by Beckman...

The Issue: Sample probes with defective probe tips, when used with clinical chemistry...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2025· Fresenius Medical Care Holdings, Inc.

Recalled Item: 5008X HDF Hemodialysis Blood Tubing Set Recalled by Fresenius Medical Care...

The Issue: Potential of blood leak occurring between the lower port of the venous...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2025· Alcon Research LLC

Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...

The Issue: Due to the potential that some units within specific lots were damaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2025· Alcon Research LLC

Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...

The Issue: Due to the potential that some units within specific lots were damaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2025· Alcon Research LLC

Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...

The Issue: Due to the potential that some units within specific lots were damaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2025· NxStage Medical Inc

Recalled Item: NxStage PureFlow-B Solution. Catalog numbers: RFP-400 Recalled by NxStage...

The Issue: Potential for the perimeter seal on the small chamber of the two-chamber bag...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2025· Abbott Molecular, Inc.

Recalled Item: Alinity m Resp-4-Plex AMP Kit Recalled by Abbott Molecular, Inc. Due to...

The Issue: There were reports of an increase in reactive negative controls and false...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2025· Abbott Molecular, Inc.

Recalled Item: Alinity m Resp-4-Plex Amplification (AMP) Kit (CE) Recalled by Abbott...

The Issue: There were reports of an increase in reactive negative controls and false...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2025· HANGZHOU ACOSOUND TECHNOLOGY CO., LTD.

Recalled Item: AcoSound. Model Number: LW12-BTE-M Recalled by HANGZHOU ACOSOUND TECHNOLOGY...

The Issue: Three issues 1. Label error: The manufacturer information in the labeling is...

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

Class III — Low RiskOngoing
Medical DeviceApril 25, 2025· Tecfen Medical

Recalled Item: Brand Name: Tecfen Medical Product Name: 3.2mm Slit Knife Recalled by Tecfen...

The Issue: Sterility assurance for Ophthalmic knives.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2025· Tecfen Medical

Recalled Item: Brand Name: Tecfen Medical Product Name: 2.0mm Crescent Knife Angled...

The Issue: Sterility assurance for Ophthalmic knives.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2025· Tecfen Medical

Recalled Item: Brand Name: Tecfen Medical Product Name: 15 degree Stab Knife Recalled by...

The Issue: Sterility assurance for Ophthalmic knives.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2025· Tecfen Medical

Recalled Item: Brand Name: Tecfen Medical Product Name: 2.8mm Slit Knife Recalled by Tecfen...

The Issue: Sterility assurance for Ophthalmic knives.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2025· GE Medical Systems Information Technologies Inc

Recalled Item: MUSE 5 Systems Recalled by GE Medical Systems Information Technologies Inc...

The Issue: The MUSE Administrator Account active directory or local credential could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2025· Tecfen Medical

Recalled Item: Brand Name: Tecfen Medical Product Name: 20G (1.2mm) MVR Sideport Recalled...

The Issue: Sterility assurance for Ophthalmic knives.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2025· Tecfen Medical

Recalled Item: Brand Name: Tecfen Medical Product Name: 2.2mm Slit Knife Recalled by Tecfen...

The Issue: Sterility assurance for Ophthalmic knives.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2025· Tecfen Medical

Recalled Item: Brand Name: Tecfen Medical Product Name: 2.4mm Slit Knife Recalled by Tecfen...

The Issue: Sterility assurance for Ophthalmic knives.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2025· Mobius Mobility LLC

Recalled Item: iBOT PMD with software version 01.05.24. Personal Mobility Device. Recalled...

The Issue: Software issue that could potentially lead to the device tipping over from...

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

Class II — Potential Health HazardOngoing