Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic… — Class II medical device recall Z-2922-2020
Terminated recall by TELEFLEX MEDICAL INC, reported 2020-09-09, distributed in AR, AZ, CA, CO, FL, GA, IA, IL…. Potential sterility issue
| Recall number | Z-2922-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | TELEFLEX MEDICAL INC, Morrisville, NC, United States |
| Recall initiated | 2020-08-07 |
| Classified | 2020-08-28 |
| Reported by FDA | 2020-09-09 |
| Terminated | 2023-01-14 |
| Distributed | AR, AZ, CA, CO, FL, GA, IA, IL, IN, LA, MI, MN, MS, NC, NH, NV, NY, OH, OK, OR, PA, SD, TN, TX, VA, WA, WI |
| Quantity | 700 eaches |
| Reason classes | sterility |
| Model numbers | DTRC-20S |
Product
Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in any surgical procedure requiring attachment to a Chest Drainage device. The thoracic catheter is indicated for use less than 30 days.
Reason for recall
Potential sterility issue
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-2922-2020. 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.