Home › ELMED INCORPORATED › ELMED
ELMED
ELMED INCORPORATED · Model 32-19-411-IV · UDI-DI 00842180162891
HDF
Prescription
10
510(k) clearances
44
Adverse events
3
Recalls
227
Facilities
Description
MEDIUM INSULATED PEDERSON VU-MORE VAGINAL SPECULUM WITH 1-5/8 WIDE YOKE 4" X 1-1/2" WITH PERMANET SMOKE EVACUTION TUBE
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
| 2023-03-16 | Carefusion 2200 Inc | A portion of the two products were incorrectly marked (etched) and packaged resulting in a product mismatch. The labels and laser etchings were switched on the two products. |
| 2019-07-01 | Centurion Medical Products Corporation | Potential for sterile packaging to be compromised |
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.