Home › Hayden Medical, Inc. › Hayden Medical
Hayden Medical
Hayden Medical, Inc. · Model L315-619 · UDI-DI 00840319732151
HDL
Prescription
2
510(k) clearances
19
Adverse events
1
Recalls
120
Facilities
Description
Redundant (Lateral) Wall Retractor 7" 17.5cm), 3-1/2" x 3/4" blades, 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. |
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.