FDA Device recall Z-0058-2021
ClearPro Closed Suction Catheter, Model DYNCPDS14T, 14 Fr FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for endotracheal su…
- FDA Device
- Class II
- terminated
- Published 2020-10-14
On 2020-10-14 the FDA classified a Class II recall of ClearPro Closed Suction Catheter, Model DYNCPDS14T, 14 Fr FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for endotracheal su… by Medline Industries, citing there have been 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-0058-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-09-01 |
| Published | 2020-10-14 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Medline Industries |
| Distribution | n/a |
Product
ClearPro Closed Suction Catheter, Model DYNCPDS14T, 14 Fr FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only.
Reason
There have been reports of the suction catheter coming apart from the device assembly during use.
Identifiers
| code_info | Model: DYNCPDS14T, Lots 06919010016 and 06919020016 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0058-2021%22
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