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Recall Observatory FDA recall evidence

Device product

AEM Disposable Electrodes, Device, Electrosurgical, Cutting and Coagulation and Accessories. AEM Disposable Electrodes used as electrosurgical accessories intended for ablation, removal, resection and coagulation of soft tissue in open, endoscopic and laparoscopic surgical procedures channeling monopolar high-frequency electrical current from compatible electrosurgical generators. The device is model FC03XX series. AEM Disposable Electrodes used as electrosurgical accessories intended for ablation, removal, resection and coagulation of soft tissue in open, endoscopic and laparoscopic surgical procedures channeling monopolar high-frequency electrical current from compatible electrosurgical generators.

Z-1951-2012

June 15, 2012

Class II

Product summary

Firm
Encision, Inc.
Event
Event 61529
Status
Terminated
Classification
Class II
Quantity
48 boxes
Official record key
device-enforcement:Z-1951-2012

Official wording

Reason: Encision is performing a field correction to their AEM Disposable Electrodes due to two consumer complaints reporting unanticipated alarms from the AEM monitor while using the device. This issue could result delays or complications during surgical procedures.

Code information: RDB, RJB, RJE, RJH, RLG, RLI, RLJ, RLK, RLO, RLP, RLR, RLQ, SBF, SBJ.

Distribution pattern: Worldwide Distribution - USA including CA, TX, GA, NY, NC, OH), and New Zealand.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Encision is performing a field correction to their AEM Disposable Electrodes due to two consumer complaints reporting unanticipated alarms from the AEM monitor while using the device. This issue could result delays or complications during surgical procedures.