Musculoskeletal Transplant Foundation, Inc. recalls QuickGraft¿ Model # 430PST
- Recall date
- August 15, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2548-2019
- FDA classification
- Class II
- Brand / firm
- Musculoskeletal Transplant Foundation, Inc.
- Sold / distributed
- NY NC LA TX MO OH
Why it was 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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
QuickGraft¿ Model # 430PST
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