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Forceps, Obstetrical

FDA product code HDA · Class 2 · Obstetrics/Gynecology

245
Registered devices
274
Adverse events
7
Recalls
10
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2019-03-13COVIDIEN LLCSterilization method used was not consistent with the labeling and the approved sterilization method
2019-03-13COVIDIEN LLCSterilization method used was not consistent with the labeling and the approved sterilization method
2019-03-13COVIDIEN LLCSterilization method used was not consistent with the labeling and the approved sterilization method
2018-12-28Fetzer Medical GmbH & Co. KGThe firm had a report of doctors being unable to pull the obstetric forceps apart.
2018-12-28Fetzer Medical GmbH & Co. KGThe firm had a report of doctors being unable to pull the obstetric forceps apart.
2018-12-28Fetzer Medical GmbH & Co. KGThe firm had a report of doctors being unable to pull the obstetric forceps apart.
2018-12-28Fetzer Medical GmbH & Co. KGThe firm had a report of doctors being unable to pull the obstetric forceps apart.

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