FDA Device recall Z-2592-2014
Split Cath III Trays, 16F x 28CM Product Usage: The Split Cath III is indicated for use in attaining long term vascular access for hemodial…
- FDA Device
- Class II
- terminated
- Published 2014-09-10
On 2014-09-10 the FDA classified a Class II recall of Split Cath III Trays, 16F x 28CM Product Usage: The Split Cath III is indicated for use in attaining long term vascular access for hemodial… by Medical Components, citing the Split Cath III Trays were incorrectly labeled as 16F x 32CM Split Cath III instead of 28CM.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2592-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-08-04 |
| Published | 2014-09-10 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Medical Components |
| Distribution | US |
Product
Split Cath III Trays, 16F x 28CM Product Usage: The Split Cath III is indicated for use in attaining long term vascular access for hemodialysis and apheresis in adult patients.
Reason
The Split Cath III Trays were incorrectly labeled as 16F x 32CM Split Cath III instead of 28CM.
Identifiers
| code_info | TRAY #55216-3; Lot numbers: MBTX960, exp. 10/2016; MBVA850, exp. 10/2016; MBVD080, exp. 01/2017; MBVG680, exp. 01/2017; MBVL020, exp. 01/2017. |
|---|
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-2592-2014%22
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