Home › SONTEC INSTRUMENTS, INC. › POMEROY EAR SYRINGE
POMEROY EAR SYRINGE
SONTEC INSTRUMENTS, INC. · Model 467-574 · UDI-DI 00192896040366
KCP
Prescription
4
510(k) clearances
26
Adverse events
1
Recalls
143
Facilities
Description
POMEROY EAR SYRINGE
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2003-04-30 | Medegen Medical Products, LLC | Finished products were not sterilized. |
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.
