Home › STERIS CORPORATION › V. Mueller
V. Mueller
STERIS CORPORATION · Model MO130-002 · UDI-DI 10885403058028
KBN
Prescription
3
510(k) clearances
47
Adverse events
1
Recalls
213
Facilities
Description
V. Mueller DINGMAN MOUTH GAG BLADE NO 1 2-1/2 inches X 1 inches 6.5 X 2.6CM WIDE
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-02-16 | Aesculap Implant Systems LLC | The plastic sleeves of the Penis Clamp and Mouth Gag may stick together during or after reprocessing rendering the instruments unusable. |
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.
