RegWardenFDA facility compliance records
Recall

Class II — EMG Technology Co., Ltd.

Recalling firmEMG TECHNOLOGY CO., LTD.
Registered facilityEMG TECHNOLOGY CO., LTD. (the firm's only registered facility)
ClassificationClass II
StatusTerminated
Reasonsuction canister lids may have occluded ports.
ProductVac-Assist Suction Units (SUA01 Suction Aspirator Unit w/800 cc Canister). The suction unit is intended for professional use to remove fluids from a patient's airway or respiratory support unit. The intended population for this device is s both adult and pediatric.
Quantity1452
DistributionUS Distribution in IL.
Initiated2014-08-03
Classified2014-09-12
Terminated2015-08-25
Recall numberZ-2642-2014
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — EMG Technology Co., Ltd. (Z-2642-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/68997/

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