FDA Device recall Z-2546-2017
USPACK-SUTURE KIT
- FDA Device
- Class II
- terminated
- Published 2017-06-21
On 2017-06-21 the FDA classified a Class II recall of USPACK-SUTURE KIT by Medtronic, citing potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2546-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-05-03 |
| Published | 2017-06-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Medtronic |
| Distribution | US |
Product
USPACK-SUTURE KIT; Item Number: US1672
Reason
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
Identifiers
| code_info | A5D0789X |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2546-2017%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.