RegWardenFDA facility compliance records
Recall

Class II — Implantech Associates Inc

Recalling firmIMPLANTECH ASSOCIATES, INC.
Registered facilityIMPLANTECH ASSOCIATES, INC. (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonImplantech initiated the voluntary recall of Gelzone Shoulder Sleever, SLV-634, Lot Number 852766 because it may not satisfy customer requirements for the robustness of the Velcro closure.
ProductGelzone Shoulder Sleeve, Catalog Number SLV634, Lot Number 852766. Product Usage: To be used where limb support and/or elevation is considered necessary.
Quantity300
DistributionWorldwide Distribution - USA (nationwide) in the states of: CA, AZ, IL, NC, CO and the country of: South Africa.
Initiated2014-01-29
Classified2014-02-20
Terminated2015-03-12
Recall numberZ-1063-2014
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 — Implantech Associates Inc (Z-1063-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/67446/

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