FDA Device Intelligence
HomeACEM SPA › ACEMST1

ACEMST1

ACEM SPA · Model ACEMST1.3 /FW · UDI-DI 08050705890231

KZF Prescription
10
510(k) clearances
401
Adverse events
5
Recalls
92
Facilities

Description

ACEMST1.3 FLEXIBLE ARM WALL

Recalls

DateFirmReason
2025-10-13MRIMed Inc.Due to battery component overheating while charging resulting in melting of internal components and causing smoke.
2017-04-21Stryker CommunicationsThe exam light may have a tolerance issue with the adapter assembly, which could potentially not allow the snap ring to be seated correctly. If this is the case, there could be in
2016-11-18Ohmeda MedicalCertain power cords could overheat. The affected power cords were manufactured by Electric-Cord and are referred to as Taller Bridge power cords. The overheating of the power cord
2013-07-25Stryker CommunicationsPotential incomplete final weld on the drop tube flange.
2004-02-19Burton Medical Products CorpPivot joint on these ceiling mount lights may fail and lights may fall onto patients.

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.