RegWardenFDA facility compliance records
Recall

Class II — North Coast Medical Inc

Recalling firmNORTH COAST MEDICAL, INC.
Registered facilityNORTH COAST MEDICAL, INC. (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonThe thumb strap of the wrist and thumb orthosis may contain latex that is not declared in the product labeling.
ProductGladiator, Wrist & Thumb Orthosis, Part Numbers: NC86650 (Small/Left), NC86651 (Small/Right), NC86652 (Medium/Left), NC86653 (Medium/Right), NC86654 (Large/Left), NC86655 (Large/Right), NC86656 (X-Large/Left), and NC86657 (X-Large/Right)
Quantity27 units
DistributionUS: NC, CA, WI OUS: New Zealand, Australia,
Initiated2023-08-18
Classified2023-10-19
Recall numberZ-0125-2024
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 — North Coast Medical Inc (Z-0125-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93079/

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