SLIM-LOC 179607016Recalls & reported problems
Depuy Spine, LLC · SLIM-LOC ANTERIOR CERVICAL PLATE SYSTEM SCREW, SELF-DRILLING 4.5 x 16mm · Class 2
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 10705034063829), received between Dec 16, 2019 and Dec 16, 2019 — 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
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 16, 2019Break; Break
DEVICE REPORT FROM (B)(6) REPORTS AN EVENT AS FOLLOWS: BREAKAGE POST-OP. IT WAS REPORTED THAT THE PATIENT UNDERWENT THE ACCF OPERATION ON (B)(6) 2015. AND NOTED THE SCREW WAS BROKEN ON (B)(6) 2019. THE RELATED PLATE IS NOT BROKEN. THE PATIENT WILL BE GIVEN THE REVISION SURGERY, BUT NOW COULD NOT CONFIRM THE SPECIFIC DATE. NOW THE PATIENT IS STABLE. CONCOMITANT DEVICES: SLIM-LOC ANTERIOR CERVICAL PLATE SYSTEM (PART: 179602045, LOT: UNKNOWN, QUANTITY: 1). THIS REPORT IS FOR A SELF-DRILLING SCREW 16MM. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: Failure of Implant; No Code Available
MAUDE report 9473304 ↗
Other APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY devices
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- EVEREST® Spinal System 2901-10001VB Spine LLC · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY119 reports
- ZEVO™ Anterior Cervical Plate System 7710015Medtronic Sofamor Danek, Inc. · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 recall1 report
- Mariner RDX MX1-000040Seaspine Orthopedics Corporation · Appliance, fixation, spinal intervertebral body1 recall0 reports
- Mariner RDX MX1-000030Seaspine Orthopedics Corporation · Appliance, fixation, spinal intervertebral body1 recall0 reports
- Elegance® Anterior Cervical Plate 53430112Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
- Elegance® Anterior Cervical Plate 53430224Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
- XLP 7565050Nuvasive, Inc. · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 recall0 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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