Stryker recalls S-Series Equipment Management System models with capacitive touch controls that may disengage when electrocautery devices are used, posing a risk of equipment malfunction during medical procedures.
The manufacturer has become aware that there is a likelihood that the S-Series Equipment Management System Capacitive Touch Controls on the MFRs rotational electrical magnetic brakes may disengage when an electrocautery device is in use.
Stryker is recalling specific S-Series Equipment Management System models due to a risk that capacitive touch controls could disengage when an electrocautery device is in use. This could lead to equipment malfunction during medical procedures, potentially affecting patient safety.
The capacitive touch controls on the S-Series Equipment Management System may disengage when an electrocautery device is in use. This disengagement could cause the equipment to malfunction during medical procedures, potentially affecting patient safety.
Healthcare professionals using Stryker S-Series Equipment Management Systems with the affected model numbers are most at risk. Patients undergoing procedures involving electrocautery devices may be impacted if the equipment malfunctions.
Check for model numbers 0682400550 and specific component serial numbers listed in the recall notice. The affected items include components like P38198, P38199, P40553, P40554, and P46269 with serial numbers 2258046 and 2863490.
Verify the model number on your S-Series Equipment Management System to see if it matches the recalled model numbers listed in the recall notice.
Reach out to Stryker Communications for guidance on the specific components affected and any necessary actions.
The affected model numbers include 0682400550 and specific components like P38198, P38199, P40553, P40554, and P46269 with serial numbers 2258046 and 2863490.
The manufacturer has become aware that the capacitive touch controls on the S-Series Equipment Management System may disengage when an electrocautery device is in use, which could lead to equipment malfunction during medical procedures.
No, the recall does not require immediate discontinuation of use. Healthcare professionals should check the model numbers and contact Stryker for guidance on necessary actions.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1297-2021 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1297-2021 from Stryker. 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.
