MAVERICK 71094111Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00885556798591), received between Sep 3, 2023 and Sep 4, 2023 — classified as 4 injuries.

The most frequently reported specific device problem is “Unintended System Motion” (4 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjurySep 4, 2023Unintended System Motion; Unintended System Motion

  IT WAS REPORTED THAT, AFTER THE PLACEMENT OF A MAVERICK EXTERNAL FIXATION SYSTEM, DURING TREATMENT, THE SURGEON STATED THAT THE MAVERICK SWIVEL ATTACHMENTS BECAME LOOSE OVER TIME. IN ORDER TO SOLVE THIS ANOTHER SURGERY WAS REQUIRED TO REPLACE THE LOOSEN MAVERICK SWIVEL ATTACHMENTS. CURRENT HEALTH STATUS OF THE PATIENT.

  Patient problems: Failure of Implant; No Clinical Signs, Symptoms or Conditions

  MAUDE report 17675147 ↗
• InjurySep 4, 2023Unintended System Motion; Unintended System Motion

  IT WAS REPORTED THAT, AFTER THE PLACEMENT OF A MAVERICK EXTERNAL FIXATION SYSTEM, DURING TREATMENT, THE SURGEON STATED THAT A MAVERICK SWIVEL ATTACHMENTS BECAME LOOSE OVER TIME. IN ORDER TO SOLVE THIS ANOTHER SURGERY WAS REQUIRED TO REPLACE THE LOOSEN MAVERICK SWIVEL ATTACHMENTS. CURRENT HEALTH STATUS OF THE PATIENT.

  Patient problems: Failure of Implant; No Clinical Signs, Symptoms or Conditions

  MAUDE report 17675134 ↗
• InjurySep 3, 2023Unintended System Motion; Unintended System Motion

  IT WAS REPORTED THAT, AFTER THE PLACEMENT OF A MAVERICK EXTERNAL FIXATION SYSTEM, DURING TREATMENT, THE SURGEON STATED THAT A MAVERICK SWIVEL ATTACHMENTS BECAME LOOSE OVER TIME. IN ORDER TO SOLVE THIS ANOTHER SURGERY WAS REQUIRED TO REPLACE THE LOOSEN MAVERICK SWIVEL ATTACHMENTS. CURRENT HEALTH STATUS OF THE PATIENT.

  Patient problems: Failure of Implant; No Clinical Signs, Symptoms or Conditions

  MAUDE report 17675118 ↗
• InjurySep 3, 2023Unintended System Motion; Unintended System Motion

  IT WAS REPORTED THAT, AFTER THE PLACEMENT OF A MAVERICK EXTERNAL FIXATION SYSTEM, DURING TREATMENT, THE SURGEON STATED THAT A MAVERICK SWIVEL ATTACHMENTS BECAME LOOSE OVER TIME. IN ORDER TO SOLVE THIS ANOTHER SURGERY WAS REQUIRED TO REPLACE THE LOOSEN MAVERICK SWIVEL ATTACHMENTS. CURRENT HEALTH STATUS OF THE PATIENT.

  Patient problems: Failure of Implant; No Clinical Signs, Symptoms or Conditions

  MAUDE report 17675116 ↗