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PROBE
KLS-Martin L.P. · Model 35-224-45-07 · UDI-DI 00888118120366
HNL
Prescription
10
510(k) clearances
40
Adverse events
1
Recalls
155
Facilities
Description
LACRIMAL, BOWMAN, NO. 4/5, DOUBLE ENDED, CYLINDRICAL
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-02-26 | Quest Medical, Inc. | Expiration date incorrectly printed in Manufacturing Date field on both pouch and carton labels |
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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.