Medicrea International recalls Medicrea Pass LP Blunt K-wire 01.6mm x 500mm-Nitinol Product reference: A06010140
- Recall date
- September 16, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0828-2020
- FDA classification
- Class II
- Brand / firm
- Medicrea International
- Sold / distributed
- Nationwide
Why it was recalled
Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the minimum tolerance axis threaded
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Medicrea Pass LP Blunt K-wire 01.6mm x 500mm-Nitinol Product reference: A06010140
Get recall alerts
Free email alert whenever Medicrea International has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Medicrea International