Home › STERIS CORPORATION › V. Mueller
V. Mueller
STERIS CORPORATION · Model OP120 · UDI-DI 10885403096495
HNC
Prescription
10
510(k) clearances
21
Adverse events
1
Recalls
189
Facilities
Description
V. Mueller GUYTON-PARK EYE SPECULUM FENESTRATED BLADES, 14MM WIDE NO LOCKING SCREWS,SUTURE POSTS WORKING LENGTH 3-3/8 inches 8.5CM
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.