Stryker's S2 Mini Drill Foot Pedal (model 1600983) may detach magnet causing uncontrolled motor start during surgery. Affected units have serial numbers starting with 16D-16I.
The magnet located inside the foot pedal may come off and may result in unattended start of unstoppable motor.
Stryker's S2 Mini Drill Foot Pedal (model 1600983) has been recalled because a magnet inside may detach and cause the drill motor to start uncontrollably during surgery. This poses a risk of unattended operation that could lead to injury.
The magnet inside the foot pedal can become dislodged during use, causing the drill motor to start without supervision. This could lead to unintended drilling actions that might injure the patient or operator.
Surgical professionals using the S2 Mini Drill System for bone drilling procedures like stapedotomy or ossiculoplasty. The risk is highest for surgeons who use the foot pedal without proper safeguards.
Check if your foot pedal has the model number 1600983 and serial numbers starting with 16D through 16I (e.g., 16D0002 to 16I0044).
Inspect the foot pedal for any signs of magnet detachment or unusual movement before use.
If the magnet appears loose or the pedal moves unexpectedly, stop using the device immediately.
The product is not safe to use as-is due to the risk of uncontrolled motor start. Affected units should be checked for magnet detachment before use.
The recall record does not specify a remedy, so contact Stryker Instruments directly for guidance on safe handling or disposal.
Affected units have the model number 1600983 and serial numbers starting with 16D through 16I (e.g., 16D0002 to 16I0044).
We’ve drafted a message you can send Bien-Air Surgery to request your refund or repair — edit it as you like.
Subject: Recall Z-0179-2021 — Bien-Air Surgery Bien-Air Surgery Hello, I own a Bien-Air Surgery that is covered by recall Z-0179-2021 from Bien-Air Surgery. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
