Home › MEDICREA INTERNATIONAL › LIGAPASS
LIGAPASS
MEDICREA INTERNATIONAL · Model B08106040S · UDI-DI 03613720191995
OWI
Prescription
1
510(k) clearances
68
Adverse events
2
Recalls
64
Facilities
Description
LIGAPASS 2.0 OPEN CONNECTOR
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-10-08 | Medicrea International | Tightening the LIGAPASS Band with this instrument, the tensioner's pliers can crush the band causing the band to break during surgery and lead to a risk of infection and re-interv |
| 2017-04-24 | OrthoPediatrics Corp | Over-tensioning of the band resulting in damage to the band causing it to rupture |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.