Home › KLS-Martin L.P. › DILATOR
DILATOR
KLS-Martin L.P. · Model 27-113-14-07 · UDI-DI 00888118054579
KCG
Prescription
1
510(k) clearances
21
Adverse events (4 deaths)
1
Recalls
87
Facilities
Description
TRACHEAL, LABORDE
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
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.