RegWardenFDA facility compliance records
Recall

Class III — Pega Medical Inc.

Recalling firmPega Medical Inc.
Registered facilityORTHOPEDIATRICS CANADA ULC (the firm's only registered facility)
ClassificationClass III
StatusTerminated
ReasonThe lot number on the pediatric orthopedic implant driver instrument handle does not match the lot number on the label.
ProductOrthopedic manual Surgical Instrument handle for Simple Locking Intra Medullary (SLIM) System - Product Usage: The SLIM handle is the grip for the SLIM driver in orthopedic surgical procedures.
Quantity3 units
DistributionUS Nationwide Distribution including in the states of Florida. No Foreign Consignees listed.
Initiated2020-04-03
Classified2020-05-15
Terminated2020-11-20
Recall numberZ-2038-2020
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 III recall — Pega Medical Inc. (Z-2038-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/85531/

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