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RecallsAboutBlog

AVID Medical, Inc.

AVID Medical, Inc.: 17 recalls listed since January 2026 across FDA; 6 rated high risk.

By year

  • 202617

By agency

  • FDA17

By category

  • Medical Device17

All recalls (17)

AVID Medical Halyard Anterior Hip Packs

The Halyard Anterior Hip Pack may contain a non-sterile component placed outside the sterile barrier.

Moderate risk, FDA, , Sterility problem

AVID Medical Custom Surgical Procedure Kits

Davinci Trucustom Bundle may be contaminated with a lubricant used during manufacturing.

Moderate risk, FDA, , Contamination

AVID Medical Halyard IV Start Kits

Halyard IV Start Kit NON-Sterile may have an open or incomplete seal on the applicator packaging.

Moderate risk, FDA, , Packaging defect

AVID Medical Halyard IV Start Kits

Halyard IV Start Kit NON-Sterile may be contaminated with Aspergillus penicillioides.

High risk, FDA, , Contamination

Halyard Medical Trays

Haylard 18G Single Shot EPI Tray may have quality and sterility issues.

High risk, FDA, , Sterility problem

AVID Medical Halyard IV Start Kits

Halyard IV Start Kit contains applicators contaminated with Aspergillus penicillioides.

High risk, FDA, , Contamination

AVID Medical Halyard IV Start Kits

The Halyard IV Start Kit lacks sterility assurance due to wrinkles in the paper lidding that may breach the seal area.

Moderate risk, FDA, , Sterility problem

Halyard Medical Convenience Kits

Halyard medical convenience kits may contain neurological sponges with unexpected variability of endotoxin levels.

Moderate risk, FDA, , Sterility problem

Halyard Total Joint and DaVinci TruCustom Bundles

Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

Moderate risk, FDA, , Labeling error

AVID Medical Halyard LAVH Packs

The Halyard Lavh Pack with Clearify Visualization System may leak because the component was sterilized against manufacturer recommendation.

Moderate risk, FDA, , Device defect

Halyard Cardiac Catheterization and Angiography Kits

Particulate within the fluid path has the potential to be introduced into blood circulation and become lodged within blood vessels.

High risk, FDA, , Foreign object

AVID Medical Halyard Standard Line Insertion Pack

The Halyard STANDARD LINE INSERTION PACK has defective silicone seals that may cause fluid occlusion or leakage.

Moderate risk, FDA, , Device defect

AVID Medical Halyard Eye Pack Convenience Kit

The Halyard Eye Pack Convenience kit contains an incorrect concentration of Betadine solution.

Moderate risk, FDA, , Device defect

Halyard Pain, Towel, Drape and Eye Bag Packs

Halyard, Pain Pack contains sealed pouches that had not undergone validated sterilization.

Moderate risk, FDA, , Sterility problem

AVID Medical Halyard Cardiac Cath and Cath Lab Kits

Halyard cardiac cath packs and kits may have a syringe adaptor that can unwind, causing loose or full disconnection.

High risk, FDA, , Device defect

Halyard Transport Bag Kit

The Halyard TRANSPORT BAG KIT has a Tyvek bag seal issue that may compromise sterility.

Moderate risk, FDA, , Sterility problem

Halyard Organ Recovery OR Pack and Mini Plus Kit South

Halyard Organ Recovery OR Pack and Halyard Mini Plus Kit South are not suitable for organ transplant.

High risk, FDA, , Device defect
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