Home › Hayden Medical, Inc. › Hayden Medical
Hayden Medical
Hayden Medical, Inc. · Model L315-119 · UDI-DI 00840319731925
HDF
Prescription
10
510(k) clearances
44
Adverse events
3
Recalls
227
Facilities
Description
Weisman-Pederson LLETZ Speculum w/ Smoke Tube, Left Open, XXL 7" x 1", NON-CONDUCTIVE
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.
