FDA Device recall Z-0105-2022
Thoraguard Chest Tube Kit, 20 Fr
- FDA Device
- Class II
- terminated
- Published 2021-10-20
On 2021-10-20 the FDA classified a Class II recall of Thoraguard Chest Tube Kit, 20 Fr by Centese, citing an adhesive joint in the SmartValve component of the device can become compromised resulting in a leak.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0105-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-08-31 |
| Published | 2021-10-20 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Centese |
| Distribution | CA |
Product
Thoraguard Chest Tube Kit, 20 Fr
Reason
An adhesive joint in the SmartValve component of the device can become compromised resulting in a leak.
Identifiers
| code_info | Model: FGS-1126 Catalog Number: TGCT120020 Lot Numbers 20100102, 21031703, and 21053102 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0105-2022%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.