# FDA recall Z-0055-2020

> **Becton Dickinson & Company** · Class II · device recall initiated 2019-05-13.

## Product

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

## 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.

## Distribution

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

## Key facts

- **Recall number:** Z-0055-2020
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-05-13
- **Report date:** 2019-10-16
- **Termination date:** 2020-08-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Franklin Lakes, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0055-2020

## Citation

> AI Analytics. FDA recall Z-0055-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0055-2020. Source: US FDA. Licensed CC0.

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