RecallRadar

FDA Device recall Z-0055-2020

BD Microtainer Tubes with LH (Lithium Heparin) Part/Catalog No.365965

On 2019-10-16 the FDA classified a Class II recall of BD Microtainer Tubes with LH (Lithium Heparin) Part/Catalog No.365965 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-0055-2020
ClassificationClass II
Statusterminated
Initiated2019-05-13
Published2019-10-16
Last updated2026-09-13 11:55 UTC
CompanyBecton Dickinson And
DistributionUS

Product

BD Microtainer Tubes with LH (Lithium Heparin) Part/Catalog No.365965

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: 811767N (01)30382903659655 (17)190930(10)811767N(30)50 (17)190930(10)811767N(30)200 (01)5038290365965…Lot Number/UDI: 811767N (01)30382903659655 (17)190930(10)811767N(30)50 (17)190930(10)811767N(30)200 (01)50382903659659 2019-09-30 815066N (01)30382903659655 (17)191130(10)815066N(30)50 (17)191130(10)815066N(30)200 (01)50382903659659 821471N (01)30382903659655 (17)200131(10)821471N(30)50 (17)200131(10)821471N(30)200 (01)50382903659659 821990N (01)30382903659655 (17)200131(10)821990N(30)50 (17)200131(10)821990N(30)200 (01)50382903659659

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-0055-2020%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.