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

Class I FDA enforcement event 87720. Recall start date: 9 Apr 2021. Status in the FDA record: Terminated. Termination date: 18 Jul 2022.

Reason for recall, in the words of FDA

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.

Class I, in the words of FDA

a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death

Avid Medical, Inc. started this device recall on 9 Apr 2021. The firm address in the FDA record is in Toano, VA. FDA put the recall in Class I. FDA event 87720 has 4 product records. The first FDA enforcement report date is 16 Jun 2021. The record gives the status Terminated, with the termination date 18 Jul 2022.

FDA enforcement report The 4 product records

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on 1 Oct 2026. openFDA export of 28 Sep 2026.

Distribution

In the words of FDA.

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

Recalling firm

Avid Medical, Inc., Toano, VA.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

4 product records in the event.

FDA event 87720: product records
Recall number	Product	Quantity	Class	Status	Report date
Z-1784-2021	ADULT CHEST TUBE TRAY. Medical convenience kit, Avid Medical Part Number: LAKC001-04	130 kits	Class I	Terminated	16 Jun 2021
Z-1785-2021	FISTULA ON-OFF KIT. Medical convenience kit, Avid Medical Part Number: MMTN020.	720 kits	Class I	Terminated	16 Jun 2021
Z-1786-2021	FISTULA (ON/OFF) ALL IN ONE BAG. Medical convenience kit, Avid Medical Part Number: VAMK024-03	160 kits	Class I	Terminated	16 Jun 2021
Z-1787-2021	DIALYSIS ACCESS Medical convenience kit, Avid Medical Part Number: VMED004-03.	560 kits	Class I	Terminated	16 Jun 2021

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class I: The highest of the three FDA recall classes.

The event in context

Device events that started in 2021: 900
Share of these events in Class I: 8%
Product records in this event: 4Median of the firm: 3
Events of the firm on the register: 24

Other events of the firm

Other FDA enforcement events of Avid Medical, Inc.
Initiated	Product (first record)	Type	Class	Records
10 Aug 2026	Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit): DPGE002-02;	Device	Class I	4
14 Jul 2026	Halyard IV Start Kit Non-Sterile REF: KRIV26-02	Device	Class II	1
14 Jul 2026	Halyard IV START KIT NON-STERILE REF: KRIV26-02	Device	Class I	1
10 Jul 2026	Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (5303907).	Device	Class II	1
9 Jul 2026	Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY 16FR W/STATLOCK Model/Catalog Number: S	Device	Class II	7
19 May 2026	Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.	Device	Class II	1
19 May 2026	Halyard medical convenience kits labeled as: 1) ENT, Model/Item Number (kit) ACEN89-01; 2) ENT, Model/Item Number (kit)	Device	Class II	3
7 May 2026	Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.	Device	Class II	1
30 Apr 2026	Halyard, Pain Pack. Kit Code: AMPK48-01.	Device	Class II	4
30 Apr 2026	Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. CARDIAC CATH PACK EAM	Device	Class I	3

Avid Medical, Inc.: all 24 events

Official channels

FDA enforcement report Z-1784-2021The FDA record of the first product of this event.
FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
FDA MedWatchThe FDA safety reporting program for drugs and medical devices.

Follow by RSS:Food, drug and device recallsFDA Class I recalls

Cite this page

Recall Register. FDA enforcement event 87720. https://recallregister.com/fda/i/87720/. Source: openFDA enforcement reports. Data through 28 Sep 2026.

Sources

Source: openFDA device enforcement reports
Licence: CC0 1.0
Export date: 28 Sep 2026
Newest FDA report date on the register: 23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?: The FDA record gives this distribution: Distributed US nationwide to TX, AZ, IL, MS, LA, MO, and TN
What quantity of product is in FDA event 87720?: The event has 4 product records. The first record gives this quantity: 130 kits
How did the recall start?: The FDA record says: Voluntary: Firm initiated
How many device recalls of 2021 have the same class?: 8% of the 900 device events that started in 2021 are in Class I.