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.
Measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure.
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.
The label measurements on the device don't account for tension, which could cause the surgical procedure to take longer than expected. Longer surgeries increase the risk of complications for patients.
Surgical teams using QuickGraft Model 430PST devices for procedures. Patients undergoing surgery with these devices may face longer procedures.
Check for serial numbers: 00319004921075, 00319004921073, 00319007681048, 00319014411085, 00618052231059, 03319006511040, 03319009191029, 03319019231072, 03519018121056.
Look for the listed serial numbers on the device to confirm if it is affected.
The label measurements don't account for tension during use, which could cause the surgical procedure to take longer than expected.
Check the serial numbers listed in the recall notice to see if your device is affected. If it is, contact the manufacturer for further instructions.
The recall is due to potential extended surgery time, not a direct risk of serious injury. The manufacturer considers this a low-risk issue.
We’ve drafted a message you can send Musculoskeletal Transplant Foundation to request your refund or repair — edit it as you like.
Subject: Recall Z-2548-2019 — Musculoskeletal Transplant Foundation Musculoskeletal Transplant Foundation Hello, I own a Musculoskeletal Transplant Foundation that is covered by recall Z-2548-2019 from Musculoskeletal Transplant Foundation. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
