AEGIS 187155024Recalls & reported problems
Depuy Spine, LLC · AEGIS ANTERIOR LUMBAR PLATE BONE SCREW 5.2 x 24mm · Class 2 · Implant
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 10705034136332), received between Aug 8, 2019 and Aug 8, 2019 — classified as 2 injuries.
The most frequently reported specific device problem is “Break” (2 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
- Break2
Patient problems
- No Code Available2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryAug 8, 2019Break; Break
L5-S1 ALIF: (B)(6) HOSPITAL, (B)(6) 2019. PATIENT CAME IN TO GET POSTERIOR STABILIZATION (DOS (B)(6) 2019) AFTER HAVING AN ALIF IN 2015. PATIENT HAD A SMALL SPONDI (SLIPPAGE OF L5 OVER S1). THE SLIPPAGE BROKE THE TWO LOWER SCREWS RATHER THAN PULLED THEM OUT. PATIENT OUTCOME: SURGEON DETERMINED THE IMPLANTS ARE OF NO DANGER OR IMPORT GIVEN THEY WERE GETTING STABILIZED IN THE BACK AS WELL. PLATE WAS STILL INTACT AND BOTH L5 SCREWS WERE HOLDING STRONG. NO SCREW BACKOUTS. PATIENT AGE: (B)(6), DOB: (B)(6). THIS COMPLAINT INVOLVES TWO (2) DEVICES.
Patient problems: No Code Available
MAUDE report 8874244 ↗InjuryAug 8, 2019Break; Break
L5-S1 ALIF: (B)(6) HOSPITAL, (B)(6) 2019. PATIENT CAME IN TO GET POSTERIOR STABILIZATION (DOS (B)(6) 2019) AFTER HAVING AN ALIF IN 2015. PATIENT HAD A SMALL SPONDI (SLIPPAGE OF L5 OVER S1). THE SLIPPAGE BROKE THE TWO LOWER SCREWS RATHER THAN PULLED THEM OUT. PATIENT OUTCOME: SURGEON DETERMINED THE IMPLANTS ARE OF NO DANGER OR IMPORT GIVEN THEY WERE GETTING STABILIZED IN THE BACK AS WELL. PLATE WAS STILL INTACT AND BOTH L5 SCREWS WERE HOLDING STRONG. NO SCREW BACKOUTS. PATIENT AGE: (B)(6), DOB: (B)(6). THIS COMPLAINT INVOLVES TWO (2) DEVICES.
Patient problems: No Code Available
MAUDE report 8874164 ↗
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- 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
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- Elegance® Anterior Cervical Plate 53430112Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
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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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