FDA Device Intelligence
Home › STERIS CORPORATION › V. Mueller

V. Mueller

STERIS CORPORATION · Model SU2856 · UDI-DI 10885403064746

HXD Prescription
10
510(k) clearances
1,252
Adverse events
4
Recalls
335
Facilities

Description

V. Mueller TUBING CLAMP FORCEPS TUBING MAX O.D. 7/8 inches 22MM withWALL 3/32 inches TO 1/8 inches OVERALL LENGTH 8 inches 20.3CM

Recalls

DateFirmReason
2025-01-31Aesculap IncThe forceps have been used in ways not covered by the design resulting in breakage of the clamps.
2024-02-23MEDLINE INDUSTRIES, LP - NorthfieldProduct may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
2018-05-04Stryker GmbHLaser etching which indicates whether the device is in compression or distraction mode appears to be on the wrong side of the lever arm
2015-06-16Symmetry Surgical, Inc.Lack of sterility assurance.

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 docs
Data 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.