Becton Dickinson & Company: Medical Device Recall in 2019 - (Recall #: Z-0055-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: May 13, 2019

Date Posted: October 16, 2019

Recall Number: Z-0055-2020

Event ID: 82851

Reason for Recall:

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.

Status: Terminated

Product Quantity: N/A

Code Information:

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

Distribution Pattern:

Nationwide Foreign: AR AU BE BN BR CA CL CN CO CR CW EC GT GY HK HN ID IN JP KR MX MY NI NZ PA PE PG PH PK SG SR SV TH TW UY VN

Voluntary or Mandated:

Voluntary: Firm initiated