FDA Device recall Z-2155-2017
CytoGuard Closed Luer Connector, Intravenous access 2 cartons of 50 units each (100 units per case)
- FDA Device
- Class II
- terminated
- Published 2017-05-31
On 2017-05-31 the FDA classified a Class II recall of CytoGuard Closed Luer Connector, Intravenous access 2 cartons of 50 units each (100 units per case) by B Braun Medical, citing B. Braun is voluntarily recalling 13 lots of CytoGuard Closed Luer Connector due to a potential for some blisters to be punctured resulting in a compromised sterility barrier.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2155-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-04-10 |
| Published | 2017-05-31 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | B Braun Medical |
| Distribution | US |
Product
CytoGuard Closed Luer Connector, Intravenous access 2 cartons of 50 units each (100 units per case)
Reason
B. Braun is voluntarily recalling 13 lots of CytoGuard Closed Luer Connector due to a potential for some blisters to be punctured resulting in a compromised sterility barrier.
Identifiers
| code_info | Lot # 1240156001, 1240156002, 1240156003, 1240156004, 1370249001, 1370251101, 1370257101, 1370259201, 1370268401, 137…Lot # 1240156001, 1240156002, 1240156003, 1240156004, 1370249001, 1370251101, 1370257101, 1370259201, 1370268401, 1370270401, 1370273801, 1470311101, and 1570315301 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2155-2017%22
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