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CHATTANOOGA

DJO, LLC · Model 3114 · UDI-DI 00888912308441

IMF
2
510(k) clearances
9
Adverse events
1
Recalls
12
Facilities

Description

C-5 220V PKG A INT'L STD

Recalls

DateFirmReason
2018-06-25DJO, LLCThe device accessories were not labeled with appropriate latex warning.

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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.