QuickGraft¿ Model # 430PST — Class II medical device recall Z-2548-2019
Terminated recall by Musculoskeletal Transplant Foundation, Inc., reported 2019-10-02, distributed in LA, MO, NC, NY, OH, TX. Measurement listed on the label is not taken under tension, and this would cause possible extension of surgica
| Recall number | Z-2548-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Musculoskeletal Transplant Foundation, Inc., Edison, NJ, United States |
| Recall initiated | 2019-08-15 |
| Classified | 2019-09-20 |
| Reported by FDA | 2019-10-02 |
| Terminated | 2020-07-01 |
| Distributed | LA, MO, NC, NY, OH, TX |
| Quantity | 9 qty |
| Reason classes | labeling |
| Serial numbers | 00319004921073, 00319004921075, 00319007681048, 00319014411085, 00618052231059, 03319006511040, 03319009191029, 03319019231072, 03519018121056 |
| Model numbers | 430PST |
Product
QuickGraft¿ Model # 430PST
Reason for recall
Measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2548-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.