Recall Z-0176-2021— Bien-Air Surgery Sa

Name: FDA recall Z-0176-2021
Creator: U.S. Food and Drug Administration
Published: 2020-09-11

Class II · Ongoing

Class II FDA medical device recall by Bien-Air Surgery Sa, initiated 2020-09-11. It names one FDA 510(k) clearance: K792159. Product: Bien-Air Surgery REF 1600407-001 SN **** FOOTCTRL OSSEODOC - Product Usage: intended to convert electrical energy to mechanically drive handpieces and microsaws used to cut and shape bones.. Reason: The magnet located inside the foot pedal may come off and may result in unattended start of unstoppable motor..

Recalling firm: Bien-Air Surgery Sa
Classification: Class II
Status: Ongoing
Initiated: 2020-09-11
Firm location: Le Noirmont, N/A, Switzerland

510(k) clearances named in this recall

1 on FDA's record

K792159 — FISCH DRILL SYSTEMJedmed Instrument Co.·cleared 1979-11-27

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Bien-Air Surgery REF 1600407-001 SN **** FOOTCTRL OSSEODOC - Product Usage: intended to convert electrical energy to mechanically drive handpieces and microsaws used to cut and shape bones.

Reason for recall

The magnet located inside the foot pedal may come off and may result in unattended start of unstoppable motor.

Data sourced from openFDA. This site is unofficial and independent of the FDA.