FDA Device recall Z-2725-2020
ClearPro Trach T-Piece Closed Suction Catheter, Model DYNCPTP14T, 14 Fr 12.5 IN FOR TRACHEOSTOMY TUBE - Product Usage: Catheters are intend…
- FDA Device
- Class II
- ongoing
- Published 2020-08-05
On 2020-08-05 the FDA classified a Class II recall of ClearPro Trach T-Piece Closed Suction Catheter, Model DYNCPTP14T, 14 Fr 12.5 IN FOR TRACHEOSTOMY TUBE - Product Usage: Catheters are intend… by Medline Industries, citing there are reports of the suction catheter coming apart from the device assembly during use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2725-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2020-06-30 |
| Published | 2020-08-05 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Medline Industries |
| Distribution | US |
Product
ClearPro Trach T-Piece Closed Suction Catheter, Model DYNCPTP14T, 14 Fr 12.5 IN FOR TRACHEOSTOMY TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only.
Reason
There are reports of the suction catheter coming apart from the device assembly during use.
Identifiers
| code_info | Model: DYNCPTP14T, Lot #6918100021: |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2725-2020%22
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