FDA Device recall Z-2922-2020
Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in any surgical procedure requiring attach…
- FDA Device
- Class II
- terminated
- Published 2020-09-09
On 2020-09-09 the FDA classified a Class II recall of Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in any surgical procedure requiring attach… by Teleflex Medical, citing potential sterility issue.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2922-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-08-07 |
| Published | 2020-09-09 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Teleflex Medical |
| Distribution | 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 |
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
Potential sterility issue
Identifiers
| code_info | 74K1900074 74K1901335 74L1901435 74M1900809 |
|---|
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-2922-2020%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.