FDA Device recall Z-0911-2013
BD Vacutainer PST Gel and Lithium Heparin (LH)
- FDA Device
- Class III
- terminated
- Published 2013-03-13
On 2013-03-13 the FDA classified a Class III recall of BD Vacutainer PST Gel and Lithium Heparin (LH) by Becton Dickinson And, citing BD is conducting a recall of the BD Vacutainer Plus Plastic Plasma Separator Tube (PST) with Light Green/BD Homogard Closure due to a deformed top of the tube reservoir reported i….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0911-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2012-03-05 |
| Published | 2013-03-13 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Becton Dickinson And |
| Distribution | US |
Product
BD Vacutainer PST Gel and Lithium Heparin (LH); 83 Units; Plus Blood Collection Tubes; Sterile; IVD; REF 367962; 4.5 mL, 13 X 100 mm; BD, Franklin Lakes, NJ USA; Made in USA. Used in hospitals, outpatient clinics and physicians' offices to collect blood from patients for specialized chemistry testing.
Reason
BD is conducting a recall of the BD Vacutainer Plus Plastic Plasma Separator Tube (PST) with Light Green/BD Homogard Closure due to a deformed top of the tube reservoir reported in two customer complaints.
Identifiers
| code_info | Reference No.: 367960; Tube Size: 13 X 75. Reference Nos. 367961-367963, and 368035; Tube Size: 13 X 100; all lots |
|---|
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-0911-2013%22
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