Reported Oct 16, 2019 · Terminated

BD MicrotainerTubes with K2E (K2EDTA) Catalog Number: 365974

Becton Dickinson & Company

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Becton Dickinson & Company · 1 Becton Dr · Franklin Lakes, NJ · 07417-1815

Is this the product you have?

  • BD MicrotainerTubes
  • with K2E (K2EDTA) Catalog Number365974
Lot codes and dates
  • Lot Number/UDI8101695 (01)30382903659747 (17)190930(10)8081695(30)50 (17)190930(10)8101695(30)200(01)50382903659741 8101696 (01)30382903659747 (17)190930(10)8081696(30)50 (17)190930(10)8101696(30)200(01)50382903659741 8101699 (01)30382903659747 (17)190930(10)8101699(30)50 (17)190930(10)8101699(30)200(01)50382903659741 8101701 (01)30382903659747 (17)190930(10)8101701(30)50 (17)190930(10)8101701(30)200(01)50382903659741 8106835 (01)30382903659747 (17)190930(10)8106835(30)50 (17)190930(10)8106835(30)200(01)50382903659741 8106837 (01)30382903659747 (17)190930(10)8106837(30)50 (17)190930(10)8106837(30)200(01)50382903659741 8106842 (01)30382903659747 (17)190930(10)8106842(30)50 (17)190930(10)8106842(30)200(01)50382903659741 8106847 (01)30382903659747 (17)190930(10)8106847(30)50 (17)190930(10)8106847(30)200(01)50382903659741 8106850 (01)30382903659747 (17)190930(10)8106850(30)50 (17)190930(10)8106850(30)200(01)50382903659741 8120851 (01)30382903659747 (17)191031(10)8120850(30)50 (17)191031(10)8120850(30)200(01)50382903659741 8121979 (01)30382903659747 (17)191031(10)8121979(30)50 (17)191031(10)8121979(30)200(01)50382903659741 8121981 (01)30382903659747 (17)191031(10)8121981(30)50 (17)191031(10)8121981(30)200(01)50382903659741 8124783 (01)30382903659747 (17)191031(10)8124783(30)50 (17)191031(10)8124783(30)200(01)50382903659741 8124880 (01)30382903659747 (17)191031(10)8124880(30)50 (17)191031(10)8124880(30)200(01)50382903659741 8127770 (01)30382903659747 (17)191031(10)8127770(30)50 (17)191031(10)8127770(30)200(01)50382903659741 8128575 (01)30382903659747 (17)191031(10)8128575(30)50 (17)191031(10)8128575(30)200(01)50382903659741 8129642 (01)30382903659747 (17)191031(10)8129642(30)50 (17)191031(10)8129642(30)200(01)50382903659741 8129645 (01)30382903659747 (17)191031(10)8129645(30)50 (17)191031(10)8129645(30)200(01)50382903659741 8197705 (01)30382903659747 (17)191231(10)8197705(30)50 (17)191231(10)8197705(30)200(01)50382903659741 8197970 (01)30382903659747 (17)191231(10)8197970(30)50 (17)191231(10)8197970(30)200(01)50382903659741 8198921 (01)30382903659747 (17)191231(10)8198921(30)50 (17)191231(10)8198921(30)200(01)50382903659741 8198927 (01)30382903659747 (17)191231(10)8198927(30)50 (17)191231(10)8198927(30)200(01)50382903659741 8243545 (01)30382903659747 (17)200229(10)8243545(30)50 (17)200229(10)8243545(30)200(01)50382903659741 8247628 (01)30382903659747 (17)200229(10)8247628(30)50 (17)200229(10)8247628(30)200(01)50382903659741 8248705 (01)30382903659747 (17)200229(10)8248705(30)50 (17)200229(10)8248705(30)200(01)50382903659741 8249986 (01)30382903659747 (17)200229(10)8249986(30)50 (17)200229(10)8249986(30)200(01)50382903659741 8288904 (01)30382903659747 (17)200331(10)8288904(30)50 (17)200331(10)8288904(30)200(01)50382903659741 8290928 (01)30382903659747 (17)200331(10)8290928(30)50 (17)200331(10)8290928(30)200(01)50382903659741"
Amount recalled
N/A

This recall covers 9 products

The agency filed one notice per product. You are reading one of them; the other 8 are below.

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Becton Dickinson & Company recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Aug 6, 2020 · Data as of Sep 19, 5:33 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.