FDA Device recall Z-2365-2021
Palindrome RT Repair Kit 15 FR TAL 23cm, Sterile, Item Code 8888541123
- FDA Device
- Class II
- ongoing
- Published 2021-09-08
On 2021-09-08 the FDA classified a Class II recall of Palindrome RT Repair Kit 15 FR TAL 23cm, Sterile, Item Code 8888541123 by Covidien, citing this voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2365-2021 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-05-28 |
| Published | 2021-09-08 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Covidien |
| Distribution | n/a |
Product
Palindrome RT Repair Kit 15 FR TAL 23cm, Sterile, Item Code 8888541123
Reason
This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
Identifiers
| code_info | Lot Numbers: 1616800188 1719300113 1828900138 2023300147 1703200130 1816400079 1833800127 2026000048 1713700156 1822000123 2009300120 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2365-2021%22
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