FDA Device recall Z-0745-2017
BD 23 G x .75 in
- FDA Device
- Class II
- ongoing
- Published 2016-12-21
On 2016-12-21 the FDA classified a Class II recall of BD 23 G x .75 in by Becton Dickinson And, citing BD has received multiple reports of units associated with the 23 G x .75 in. BD Vacutainer¿ Push Button Blood Collection Set with 12 in. Tubing whose lots are exhibiting separatio….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0745-2017 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2016-08-08 |
| Published | 2016-12-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Becton Dickinson And |
| Distribution | US |
Product
BD 23 G x .75 in. BD Vacutainer¿ Push Button Blood Collection Set with 12 in. Tubing Catalog # 367342 Intended for venipuncture to obtain blood specimens from patients.
Reason
BD has received multiple reports of units associated with the 23 G x .75 in. BD Vacutainer¿ Push Button Blood Collection Set with 12 in. Tubing whose lots are exhibiting separation of front and rear barrels upon activation of the safety feature, which retracts the needle.
Identifiers
| code_info | 5355531 5355533 5356681 5356682 6006629 6006630 6006631 6006633 6006634 6006650 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0745-2017%22
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