ClearPro Closed Suction Catheter — Class II medical device recall Z-0058-2021
Terminated recall by Medline Industries Inc, reported 2020-10-14. There have been reports of the suction catheter coming apart from the device assembly during use.
| Recall number | Z-0058-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries Inc, Northfield, IL, United States |
| Recall initiated | 2020-09-01 |
| Classified | 2020-10-06 |
| Reported by FDA | 2020-10-14 |
| Terminated | 2022-05-27 |
| Quantity | 6,225 units |
| Lot numbers | 06919010016, 06919020016 |
| Model numbers | 06919010016, 06919020016, DYNCPDS14T |
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 for recall
There have been reports of the suction catheter coming apart from the device assembly during use.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0058-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.