MOSS 179762040Recalls & reported problems
Depuy Spine, LLC · MOSS MIAMI SPINE SYSTEM ROD 5.5 x 40mm · Class 2 · Implant
All models of MOSS (16)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10705034077307), received between Jan 6, 2022 and Jan 6, 2022 — classified as 2 injuries.
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
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Osteolysis2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJan 6, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN (B)(6) AS FOLLOWS: IT WAS REPORTED THAT ON (B)(6) 2016, THE PATIENT UNDERWENT A PRIMARY POSTERIOR LUMBAR INTERBODY FUSION (PLIF) (L4-5) PROCEDURE. ON (B)(6) 2021, IT WAS REPORTED THAT THE PATIENT HAD SUFFERED FROM ASD BETWEEN L3-4. THE PATIENT WAS SCHEDULED TO UNDERGO A REVISION PROCEDURE (L3-4 PLIF EXTENSION) ON (B)(6) 2021. NO FURTHER INFORMATION IS AVAILABLE. THIS REPORT IS FOR ONE (1) MOSS MIAMI SPINE SYSTEM ROD 5.5 X 40MM. THIS IS REPORT 8 OF 12 FOR COMPLAINT (B)(4).
Patient problems: Osteolysis
MAUDE report 13176835 ↗InjuryJan 6, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN (B)(6) AS FOLLOWS: IT WAS REPORTED THAT ON (B)(6) 2016, THE PATIENT UNDERWENT A PRIMARY POSTERIOR LUMBAR INTERBODY FUSION (PLIF) (L4-5) PROCEDURE. ON (B)(6) 2021, IT WAS REPORTED THAT THE PATIENT HAD SUFFERED FROM ASD BETWEEN L3-4. THE PATIENT WAS SCHEDULED TO UNDERGO A REVISION PROCEDURE (L3-4 PLIF EXTENSION) ON (B)(6) 2021. NO FURTHER INFORMATION IS AVAILABLE. THIS REPORT IS FOR ONE (1) MOSS MIAMI SPINE SYSTEM ROD 5.5 X 40MM. THIS IS REPORT 5 OF 12 FOR COMPLAINT (B)(4).
Patient problems: Osteolysis
MAUDE report 13176818 ↗
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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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