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FDA Medical Device Recalls (openFDA)

Becton Dickinson & Company: BD Vacutainer Blood Transfer Device. It consists of a Luer attached via a hub to a needle covered with a sleeve.

Recall number
Z-1423-05
Recalling firm
Becton Dickinson & Company
Product
BD Vacutainer Blood Transfer Device. It consists of a Luer attached via a hub to a needle covered with a sleeve.
Status
Terminated
Initiated
2005-07-11
Posted
2005-08-30
Terminated
2006-06-29
Reason
Customer complaints state the needle had separated from the hub, resulting in blood exposure and/or dislocation of the needle.
Root cause
Other
Action
A customer communication was sent by first class mail on 7/26/05, advising all consignees of the problem. The letter asks each customer to immediately examine their inventory for affected lot numbers, return product from affected lots using enclosed label and packing slip, and to notify all of their affected customers to alert them to the situation.
Quantity
641200 eaches
Distribution
Worldwide
Lot, serial or model codes
Catalog #364880, Lot #5076799, Exp 2/2008; #50076797, exp. 2/2008; #5976798, Exp 2/2008; #5098260, Exp 3/2008; #5112114, Exp 3/2008.
510(k) numbers
["K990188"]
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

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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

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