FDA Device recall Z-2548-2019
QuickGraft¿ Model # 430PST
- FDA Device
- Class II
- terminated
- Published 2019-10-02
On 2019-10-02 the FDA classified a Class II recall of QuickGraft¿ Model # 430PST by Musculoskeletal Transplant Foundation, citing measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2548-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-08-15 |
| Published | 2019-10-02 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Musculoskeletal Transplant Foundation |
| Distribution | LA, MO, NC, NY, OH, TX |
Product
QuickGraft¿ Model # 430PST
Reason
Measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure.
Identifiers
| code_info | Serial # 00319004921075 00319004921073 00319007681048 00319014411085 00618052231059 03319006511040 03319009191029 03319019231072 03519018121056 |
|---|
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-2548-2019%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.