RecallRadar

FDA Device recall Z-0054-2020

BD Microtainer Z (No Additive Tubes) Part/Catalog No.365963

On 2019-10-16 the FDA classified a Class II recall of BD Microtainer Z (No Additive Tubes) Part/Catalog No.365963 by Becton Dickinson And, citing damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0054-2020
ClassificationClass II
Statusterminated
Initiated2019-05-13
Published2019-10-16
Last updated2026-09-13 11:55 UTC
CompanyBecton Dickinson And
DistributionUS

Product

BD Microtainer Z (No Additive Tubes) Part/Catalog No.365963

Reason

Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.

Identifiers

code_info
Lot Number/UDI: 8117750 (01)30382903659631 (17)191031(10)8117750(30)50 (17)191031(10)8117750(30)200 (01)5038290365963…Lot Number/UDI: 8117750 (01)30382903659631 (17)191031(10)8117750(30)50 (17)191031(10)8117750(30)200 (01)50382903659635 8155792 (01)30382903659631 (17)191130(10)8155792(30)50 (17)191130(10)8155792(30)200 (01)50382903659635 8223778 (01)30382903659631 (17)200131(10)8223778(30)50 (17)200131(10)8223778(30)200 (01)50382903659635 8223779 (01)30382903659631 (17)200131(10)8223779(30)50 (17)200131(10)8223779(30)200 (01)50382903659635 8268514 (01)30382903659631 (17)200229(10)8268514(30)50 (17)200229(10)8268514(30)200 (01)50382903659635

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0054-2020%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.