RegWardenFDA facility compliance records
Recall

Class II — Southwest Technologies Inc

Recalling firmSOUTHWEST TECHNOLOGIES, INC.
Registered facilitySOUTHWEST TECHNOLOGIES, INC. (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonElasto-Gel Wound Dressing may be contaminated with mold.
ProductElasto-Gel Absorbent Wound Dressing, Item DR8000. 5 Dressings 4" x 4". Sterile. UPC 45713-58000 Bacteriostatic
Quantity3260 eaches (5 eaches per retail box)
DistributionCA, GA, IL, KS, NY, OH, TN, TX, VA
Initiated2019-11-18
Classified2019-12-13
Terminated2024-08-23
Recall numberZ-0687-2020
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 — Southwest Technologies Inc (Z-0687-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/84293/

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