Drug recall

Stryker Visum 300 Ceiling-mounted Exam Light.

FDA recall event 65888 · Class II · Stryker Communications

Key facts

Event ID 65888
Recall numbers Z-1992-2013
Recalling firm Stryker Communications
Product type Devices
Products Stryker Visum 300 Ceiling-mounted Exam Light.
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Potential incomplete final weld on the drop tube flange.
Initiation date Jul 25, 2013
Report date Aug 28, 2013
Termination date Apr 3, 2015
City Flower Mound
State TX
Country United States
FEI number 3002975342

At a glance

  • 1–9 Products in this recall
  • 1–9 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date:

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