FDA Device recall Z-1684-2017
Cyto-Chex BCT - blood specimen collection device - Immunophenotyping Preservative
- FDA Device
- Class II
- ongoing
- Published 2017-04-05
On 2017-04-05 the FDA classified a Class II recall of Cyto-Chex BCT - blood specimen collection device - Immunophenotyping Preservative by Streck, citing complaints of the 2.0ml tube stopper coming loose during phlebotomy when small diameter tube adapters were not utilized. Such adapters aid with centering small diameter tubes to p….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1684-2017 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2017-02-23 |
| Published | 2017-04-05 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Streck |
| Distribution | US |
Product
Cyto-Chex BCT - blood specimen collection device - Immunophenotyping Preservative. IVD. Sterile. 2.0ml only. Packaged 6-tube pack REF 213559 and 100-tube box REF 218980. Streck.
Reason
Complaints of the 2.0ml tube stopper coming loose during phlebotomy when small diameter tube adapters were not utilized. Such adapters aid with centering small diameter tubes to properly pierce the middle of the stoppers.
Identifiers
| code_info | UDI Number 10844509000836 and 20844509000833. Lot(s) Expiration Date 50910309 04-01-…UDI Number 10844509000836 and 20844509000833. Lot(s) Expiration Date 50910309 04-01-2017 60760309 03-16-2018 61460309 05-25-2018 |
|---|
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-1684-2017%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.