FDA Medical Device Recalls (openFDA)
Becton Dickinson & Company: BD MicrotainerTubes with K2E (K2EDTA) Catalog Number: 365974
- Recall number
- Z-0057-2020
- Recalling firm
- Becton Dickinson & Company
- Product
- BD MicrotainerTubes with K2E (K2EDTA) Catalog Number: 365974
- Status
- Terminated
- Initiated
- 2019-05-13
- Posted
- not on file
- Terminated
- 2020-08-06
- 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.
- Root cause
- Process control
- Action
- Becton Dickinson (BD) notified consignees affected by letter via UPS and email dated May 13,2019. Letter describes reason for recall, health risk and action to take: 1. Immediately review your inventory for the specific catalog and lot numbers listed below, 2. Destroy all product subject to the recall following your institution's process for destruction, 3. Share this Urgent Medical Device Recall notification with all users of the product to ensure that they are also aware of this recall, and 4. Complete the attached Customer Response/Certificate of Destruction Forms and return to the BD contact noted on the form whether or not you have any of the impacted material so that BD may acknowledge your receipt of this notification and process your product replacement. Distributors provide their customer list to BD. BD PAS will notify these customers via mail. BD Contact US Contact Information Customer/Technical Support 888-237-2762 OPT 3, OPT 2; Monday Friday 8:00am - 5:00pm (CT).
- Quantity
- not on file
- 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
- Lot, serial or model codes
- Lot Number/UDI: 8101695 (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"
- 510(k) numbers
- ["K002456","K991702"]
- PMA numbers
- not on file
- Product code
- JKA
- Firm FEI
- 2243072
- Firm city
- Franklin Lakes
- Firm state
- NJ
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28