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MAC TITANIUM 48213038Recalls & reported problems

Stryker Corporation · 39 - 43 mm M.A.C. Connector · Class 2 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613154345076), received between Feb 5, 2016 and Feb 5, 2016 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (1 report).

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

Device problems

  • Break1
  • Failure To Adhere Or Bond1
  • Fracture1

Patient problems

  • Injury1
  • No Information1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryFeb 5, 2016Fracture; Failure To Adhere Or Bond; Break; Fracture

    IT WAS REPORTED THAT THE PATIENT HAD A PREVIOUS SURGERY FROM T10-L5. DR. SAID THAT HE WAS NOT FUSED AT L2-3 WHERE BOTH RODS BROKE. THE CROSSLINK ALSO BROKE. BOTH RODS AND CROSSLINK WERE REPLACED.

    Patient problems: Injury; No Information

    MAUDE report 5413789 ↗

Other APPLIANCE, FIXATION, SPINAL INTERLAMINAL devices

All APPLIANCE, FIXATION, SPINAL INTERLAMINAL devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.