MOSS 175568000Recalls & reported problems
Depuy Spine, LLC · MOSS MIAMI SPINE SYSTEM STAPLE WASHER 5.5 · Class 2
All models of MOSS (16)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 10705034034126), received between Nov 8, 2017 and Nov 8, 2017 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- Failure of Implant1
- Injury1
- Nonunion/Delayed-union Bone Fracture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 8, 2017Break; Break
NON UNION AT L3/BROKEN SCREW - ANTERIOR SCOLIOSIS PSF. CONGENITAL SCOLIOSIS. REVISION OF THE ANTERIOR FUSION (T11-L3) OF AN ANTERIOR/POSTERIOR SCOLIOSIS FUSION. ORIGINAL SURGERY PERFORMED IN 2007. PATIENT PRESENTED WITH A NON UNION AT L3 AND A BROKEN SCREW AT L3. THE SURGEON IS NOT SURE WHICH OCCURRED 1ST. THE BROKEN HEAD OF THE SCREW, MONOAXIAL SCREW AT L2, SINGLE STAPLE (X 1), SET SCREWS (X5) AND SINGLE ROD WERE REMOVED. THE SURGEON WAS UNABLE TO REMOVE THE SHAFT OF THE SCREW AT L3. SCREW REMOVED AND REPLACED AT L2 AND THEN PLACED ANOTHER SCREW, BESIDE L2 AND L3. A ROD WAS THEN PLACED IN T11-L3 AND IN THE NEW SCREWS, L2 AND L3. HE ALSO PLACED A MESH CAGE IN THE DISC SPACE BETWEEN L2 AND L3 TO ASSIST WITH SCOLIOSIS. PHOTOS OF X-RAYS, EXPLANTED IMPLANTS AND POST OP PHOTO OF THE X-RAY
Patient problems: Failure of Implant; Injury; Nonunion/Delayed-union Bone Fracture
MAUDE report 7008988 ↗
Other APPLIANCE, FIXATION, SPINAL INTERLAMINAL devices
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- EXPEDIUM VERSE 199721001Medos International Sàrl · APPLIANCE, FIXATION, SPINAL INTERLAMINAL227 reports
- XIA 3 48230000Stryker Corporation · APPLIANCE, FIXATION, SPINAL INTERLAMINAL193 reports
- VIPER 186715000Medos International Sàrl · APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 death167 reports
- NA 04.614.014Synthes GmbH · APPLIANCE, FIXATION, SPINAL INTERLAMINAL80 reports
- EXPEDIUM VIPER 196789480Depuy Spine, LLC · APPLIANCE, FIXATION, SPINAL INTERLAMINAL72 reports
- NA 04.615.014Synthes GmbH · APPLIANCE, FIXATION, SPINAL INTERLAMINAL72 reports
- Arsenal Deformity Spinal Fixation System 47127Alphatec Spine, Inc. · APPLIANCE, FIXATION, SPINAL INTERLAMINAL66 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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