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ACCULIF 400010Recalls & reported problems

Stryker Corporation · PL CAGE · Class 2 · Implant

All models of ACCULIF (15)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
7
Deaths reported
0
Injuries reported
7
Recalls naming it
0

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 07613327066777), received between Mar 3, 2016 and Nov 15, 2016 — classified as 7 injuries.

The most frequently reported specific device problem is “Collapse” (6 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Collapse6
  • Mechanical Problem6
  • Migration or Expulsion of Device2
  • Device Dislodged or Dislocated1

Patient problems

  • Injury6
  • No Code Available4
  • No Information1
  • No Known Impact Or Consequence To Patient1
  • Pain1

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

  • InjuryNov 15, 2016Mechanical Problem; Collapse; Mechanical Problem

    IT WAS REPORTED THAT; DURING SURGERY, AN IMPLANT COLLAPSED AFTER THE SURGEON HAD EXPANDED IT IN A POST-OP MRI. UPDATE (B)(6) 2016 PATIENT RECEIVED A REVISION SURGERY.

    Patient problems: Injury; No Code Available

    MAUDE report 6104708 ↗
  • InjurySep 30, 2016Mechanical Problem; Collapse; Mechanical Problem

    IT WAS REPORTED THAT; COLLAPSE NOTICED ON FOLLOW UP VISIT XRAY. UPDATE: (B)(6) 2106 - MILD BACK PAIN.

    Patient problems: Pain

    MAUDE report 5991949 ↗
  • InjuryJul 6, 2016Collapse; Mechanical Problem; Mechanical Problem

    IT WAS REPORTED THAT; DOCTOR WAS PERFORMING A REVISION ALIF AND REMOVED A CAGE THAT HAD COLLAPSED.

    Patient problems: Injury; No Code Available

    MAUDE report 5772014 ↗
  • InjuryJun 21, 2016Collapse; Migration or Expulsion of Device; Device Dislodged or Dislocated; Device Dislodged or Dislocated

    IT WAS REPORTED THAT; THE PATIENT RECEIVED A CAGE FOR A TLIF AND THE CAGE COLLAPSED POSTOPERATIVELY. UPDATE (B)(6) 2016: SPOKE TO THE REP AND HE INDICATED THAT THE CAGE HAS NOW BACKED OUT. UPDATE (B)(6) 2016: THE REVISION SURGERY PERFORMED ON (B)(6) 2016 DUE IMPLANT MIGRATION. PATIENT DID NOT REPORT ANY PAIN PRIOR THE IMPLANT MIGRATION WAS NOTICED.

    Patient problems: Injury; No Code Available

    MAUDE report 5740186 ↗
  • InjuryApr 18, 2016Collapse; Mechanical Problem; Mechanical Problem

    IT WAS REPORTED THAT THE CAGE COLLAPSED.

    Patient problems: Injury; No Known Impact Or Consequence To Patient

    MAUDE report 5585487 ↗
  • InjuryMar 8, 2016Mechanical Problem; Mechanical Problem; Migration or Expulsion of Device

    IT WAS REPORTED THAT UPON POST OP FOLLOW UP, PHYSICIAN FELT THAT THE CAGE HAD MIGRATED POSTERIORLY. REVISION SURGERY DONE ON (B)(6) 2015 TO REMOVE THE CAGE.

    Patient problems: Injury; No Code Available

    MAUDE report 5485783 ↗
  • InjuryMar 3, 2016Mechanical Problem; Collapse; Mechanical Problem

    IT WAS REPORTED THAT UPON POST-OP FOLLOW UP, SURGEON DETERMINED VIA X RAY THAT THE CAGE APPEARED TO HAVE COLLAPSED.

    Patient problems: Injury; No Information

    MAUDE report 5478539 ↗

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Sources and updates

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