RegWardenFDA facility compliance records
Facility

MEDSHAPE, INC.

2 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2019: 1 inspections; 2021: 1 recalls; 2025: 1 recalls; 2026: 1 inspections20172018120192020120212022202320241202512026
  • Recalls (2)
  • Inspections (2)

Devices registered here (1)

Recalls & enforcement

  • Class IIOngoing2025-06-02
    Bone external fixation system may have the pin that can become dislodged resulting in frame instability, the use of this product may cause a delay in surgery or a revision if the device is use.
  • Class IIOngoing2021-11-17
    The firm identified a nonconformance in Lot 04882 involving the endcap being manufactured to a longer length than indicated in product specifications, introducing the risk of the +6 mm endcap not seating flush with the nail while inserting during a procedure.

FDA inspections (2)

  • NAI2026-02-13
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
  • NAI2019-04-16
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

Related

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

Cite this record

RegWarden. “MEDSHAPE, INC. (FEI 3007593722) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3007593722-medshape-inc/

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