OsteoBridge Intramedullary Diaphysis Segment Fixation nails recalled over labeling errors
- Recall date
- September 18, 2020
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Merete Medical GmbH recalls OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (humerus)
- Recall number
- Z-0438-2021
- FDA classification
- Class II
- Brand / firm
- Merete Medical GmbH
- Sold / distributed
- Product was distributed in US - CA, IL, MD, OH, and NJ
Why it was recalled
Product may be mislabeled.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (humerus)
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