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Recorder, Paper Chart

FDA product code DSF · Class 1 · Cardiovascular

1,331
Registered devices
6
Adverse events
1
Recalls
87
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2015-12-02Gsi Group IncThe item was recalled due to an increased user/patient risk of exposure to fire and/or electrical shock due to the failure of the PRN 50-M+ Digital Writer

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.