Dawson-Mueller Drainage Catheter — Class II medical device recall Z-0815-2020
Terminated recall by Cook Inc., reported 2020-01-22, distributed nationwide. Specific lots of the Dawson-Mueller Drainage Catheter were not manufactured to specification, which could lead
| Recall number | Z-0815-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cook Inc., Bloomington, IN, United States |
| Recall initiated | 2019-12-27 |
| Classified | 2020-01-16 |
| Reported by FDA | 2020-01-22 |
| Terminated | 2020-11-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BE, CA, CN, CO, DE, DK, ES, FR, GB, IT, KR, NL, NZ, PE, RU, SE |
| Quantity | 1,604 |
| Reason classes | packaging |
Product
Dawson-Mueller Drainage Catheter, Multipurpose Drainage Catheter, RPN UL T6.3-35-15-P-5S-CLDM-HC, UL T6. 3-35-25-P-58-CLDM-HC, UL T7.0-35-25-P-5S-CLDM-HC
Reason for recall
Specific lots of the Dawson-Mueller Drainage Catheter were not manufactured to specification, which could lead to leakage from the Mac-Loc hub assembly.
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-0815-2020. 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.