FDA Device recall Z-0756-2013
BD Vacutainer Buffered Sodium Citrate (9NC) Plus Blood Collection Tubes
- FDA Device
- Class II
- terminated
- Published 2013-02-06
On 2013-02-06 the FDA classified a Class II recall of BD Vacutainer Buffered Sodium Citrate (9NC) Plus Blood Collection Tubes by Becton Dickinson And, citing BD is conducting a recall of the BD Vacutainer 2.7mL Plus Citrate Blood Collection Tube due to extended Partial Thromboplastin Time (aPTT) test results reported in two customer co….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0756-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-11-12 |
| Published | 2013-02-06 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Becton Dickinson And |
| Distribution | US |
Product
BD Vacutainer Buffered Sodium Citrate (9NC) Plus Blood Collection Tubes; Sterile; IVD; REF 363083; 13 X 75 mm, 2.7 mL
Reason
BD is conducting a recall of the BD Vacutainer 2.7mL Plus Citrate Blood Collection Tube due to extended Partial Thromboplastin Time (aPTT) test results reported in two customer complaints.
Identifiers
| code_info | Lot No. 2180434; Expiration Date: April 2013 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0756-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.