FDAOctober 11, 2019device

Berchtold Chromophare Ceiling Mounted Surgical Light System, Catalog #CH13000000

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The firm has become aware that there is a likelihood that a missing snap ring or spanner nut may result in an insufficient mount force that causes the surgical light to fall. If the suspension of the surgical light falls, it may potentially cause serious injuries to Health Care Providers and/or patients.

What to do

FDA enforcement status: Terminated

Brands named

stryker communicationsstryker

UPCs

0913167001608311773252

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Berchtold Chromophare Ceiling Mounted Surgical Light System, Catalog #CH13000000 — Recall Details · AllClear