RecallRadar

FDA Device recall Z-1787-2021

DIALYSIS ACCESS Medical convenience kit, Avid Medical Part Number: VMED004-03

On 2021-06-16 the FDA classified a Class I recall of DIALYSIS ACCESS Medical convenience kit, Avid Medical Part Number: VMED004-03 by Avid Medical, citing 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 ap….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1787-2021
ClassificationClass I
Statusterminated
Initiated2021-04-09
Published2021-06-16
Last updated2026-09-13 11:56 UTC
CompanyAvid Medical
DistributionUS

Product

DIALYSIS ACCESS Medical convenience kit, Avid Medical Part Number: VMED004-03.

Reason

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.

Identifiers

code_info
Part Number:VMED004-03; Package GTIN: 20809160238247; Lot Number: 1409970 (Expiration Date: 04/26/2022), 1412734 (Expir…Part Number:VMED004-03; Package GTIN: 20809160238247; Lot Number: 1409970 (Expiration Date: 04/26/2022), 1412734 (Expiration Date: 10/01/2021), 1413146 (Expiration Date: 10/01/2021), and 1413395 (Expiration Date: 04/25/2022)

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1787-2021%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.