Avid Medical, Inc.: Medical Device Recall in 2021 - (Recall #: Z-1784-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

ADULT CHEST TUBE TRAY. Medical convenience kit, Avid Medical Part Number: LAKC001-04

Product Classification:

Class I

Date Initiated: April 9, 2021

Date Posted: June 16, 2021

Recall Number: Z-1784-2021

Event ID: 87720

Reason for Recall:

Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. Under certain circumstances the applicator may grow Aspergillus penicillioides, which may result in a breach of the package integrity. A breach of package integrity may contaminate other components in AVID Medical kits.

Status: Terminated

Product Quantity: 130 kits

Code Information:

Part Number: LAKC001-04; Package GTIN: 20809160261016; Lot Number: 1404809 (Expiration Date: 08/01/2021) and 1408337 (Expiration Date: 09/01/2021) Part Number: LAKC001-04; Package GTIN: 20809160293130; Lot Number: 1427628 (Expiration Date: 09/01/2021) Part Number: LAKC001-04; Package GTIN: 20809160313005; Lot number: 1427629 (Expiration Date: 09/01/2021), 1432814 (Expiration Date: 11/30/2021), and 1436046 (Expiration Date: 11/30/2021)

Distribution Pattern:

Distributed US nationwide to TX, AZ, IL, MS, LA, MO, and TN

Voluntary or Mandated:

Voluntary: Firm initiated