Lower risk Medical device recall · FDA · Published August 15, 2019

QuickGraft Model 430PST: Possible extended surgery time due to measurement error

Musculoskeletal Transplant Foundation recalls QuickGraft Model 430PST due to label measurements not accounting for tension, potentially increasing surgical time. Affected units have specific serial numbers listed.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2548-2019Medical device Musculoskeletal Transplant Foundation ›

Lower-risk 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.

Take action

Contact the company

Recalling firmMusculoskeletal Transplant Foundation, Inc.125 May St Ste 300 · Edison, NJ 08837-3264

✎ GovInfoNow plain-language explainer

Musculoskeletal Transplant Foundation recalls QuickGraft Model 430PST surgical devices because the label measurements don't account for tension during use. This could lead to longer surgery times, which may increase risks for patients. Read more at govinfonow.com/recall/67181-quickgraft-model-430pst-possible-extended-surgery-time-due-to-measurement.

Source Summary by GovInfoNow · govinfonow.com/recall/67181-quickgraft-model-430pst-possible-extended-surgery-time-due-to-measurement · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2548-2019

Cite this page

“QuickGraft Model 430PST: Possible extended surgery time due to measurement error.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/67181-quickgraft-model-430pst-possible-extended-surgery-time-due-to-measurement. Based on FDA recall #Z-2548-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2548-2019%22&limit=1).

The FDA announced on 2019-08-15 that Musculoskeletal Transplant Foundation, Inc. voluntarily recalled QuickGraft Model # 430PST devices because the labeled measurement was not taken under tension, potentially extending surgical time.

How to tell if you have it

Brand: Musculoskeletal Transplant Foundation
Product: QuickGraft Model # 430PST
Serial numbers: 00319004921075, 00319004921073, 00319007681048, 00319014411085, 00618052231059, 03319006511040, 03319009191029, 03319019231072, 03519018121056
Quantity: 9 units
Distribution states: NY, NC, LA, TX, MO, OH

The hazard

The FDA stated that the measurement listed on the label is not taken under tension, which would cause possible extension of surgical time needed to complete the procedure.

Context

GovInfoNow's records show Musculoskeletal Transplant Foundation, Inc. has had three other recalls since 2021-03-29. Other recent recalls of similar products include XTANT Medical Xpress Pedicle Screw System (2026-02-18), F & A Foundation Reign Medical Clench Staple System Recall (2026-07-15), and Grace Medical Stapes Prosthesis recall (2026-04-03).

How to tell if you have this one

Check for serial numbers: 00319004921075, 00319004921073, 00319007681048, 00319014411085, 00618052231059, 03319006511040, 03319009191029, 03319019231072, 03519018121056.

Brand
Musculoskeletal Transplant Foundation
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Serial Numbers
Look for the listed serial numbers on the device to confirm if it is affected.

Where it went and when

Where it was distributed

Distributed in 6 states.

FDA distribution: “NY NC LA TX MO OH” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Louisiana, Missouri, New York, North Carolina, Ohio, Texas.

Recall timeline

FDA terminated this recall 11 months after the firm started it.

Aug 15, 2019Firm started the recall
Sep 20, 2019FDA classified it Class II
Oct 2, 2019Published in FDA’s Enforcement Report
Jul 1, 2020FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

Is there a risk of serious injury?

The recall is due to potential extended surgery time, not a direct risk of serious injury. The manufacturer considers this a low-risk issue.

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Link to this recall

<a href="https://govinfonow.com/recall/67181-quickgraft-model-430pst-possible-extended-surgery-time-due-to-measurement">QuickGraft Model 430PST: Possible extended surgery time due to measurement error (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-2548-2019 (August 15, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2548-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.