FDA Device recall Z-2724-2020
ClearPro T-Piece Closed Suction Catheter, Model DYNCPTP14, 14 Fr 21.3 IN FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for…
- FDA Device
- Class II
- ongoing
- Published 2020-08-05
On 2020-08-05 the FDA classified a Class II recall of ClearPro T-Piece Closed Suction Catheter, Model DYNCPTP14, 14 Fr 21.3 IN FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for… 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-2724-2020 |
| 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 T-Piece Closed Suction Catheter, Model DYNCPTP14, 14 Fr 21.3 IN FOR ENDOTRACHEAL 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: DYNCPTP14, Lot #6919020016: |
|---|
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-2724-2020%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.