Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

QuickGraft¿ Model # 430PST Recalled by Musculoskeletal Transplant Foundation, Inc. Due to Measurement listed on the label is not taken...

Date: August 15, 2019
Company: Musculoskeletal Transplant Foundation, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Musculoskeletal Transplant Foundation, Inc. directly.

Affected Products

QuickGraft¿ Model # 430PST

Quantity: 9 Qty

Why Was This Recalled?

Measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure.

Where Was This Sold?

This product was distributed to 6 states: LA, MO, NY, NC, OH, TX

Affected (6 states)Not affected

About Musculoskeletal Transplant Foundation, Inc.

Musculoskeletal Transplant Foundation, Inc. has 9 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report