EAGLE SWIFT 286560000Recalls & reported problems
Depuy Spine, LLC · EAGLE/SWIFT PLUS ANTERIOR CERVICAL PLATE SYSTEM THREADED DRIVER x15 · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10705034213088), received between Dec 21, 2017 and Dec 21, 2017 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (3 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
- Break3
Patient problems
- No Consequences Or Impact To Patient3
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 21, 2017Break; Break
THE SURGEON WAS RE-POSITIONING A PLATE. HE HAD A DIFFICULT TIME REMOUNTING THE SCREWS AND BROKE OR STRIPPED SOME OF THE DRIVERS. UPON INSPECTION SOME OF THE THREADS ON THE SCREWS WERE MESSED UP SO THE SURGEON DID NOT FEEL COMFORTABLE PUTTING THOSE BACK IN AND THAT THEY WOULD STILL BE BLOCKED BY THE CLOCKING RING.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7138770 ↗MalfunctionDec 21, 2017Break; Break
THE SURGEON WAS RE-POSITIONING A PLATE. HE HAD A DIFFICULT TIME REMOUNTING THE SCREWS AND BROKE OR STRIPPED SOME OF THE DRIVERS. UPON INSPECTION SOME OF THE THREADS ON THE SCREWS WERE MESSED UP SO THE SURGEON DID NOT FEEL COMFORTABLE PUTTING THOSE BACK IN AND THAT THEY WOULD STILL BE BLOCKED BY THE CLOCKING RING.
Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient
MAUDE report 7138384 ↗MalfunctionDec 21, 2017Break; Break
THE SURGEON WAS RE-POSITIONING A PLATE. HE HAD A DIFFICULT TIME REMOUNTING THE SCREWS AND BROKE OR STRIPPED SOME OF THE DRIVERS. UPON INSPECTION SOME OF THE THREADS ON THE SCREWS WERE MESSED UP SO THE SURGEON DID NOT FEEL COMFORTABLE PUTTING THOSE BACK IN AND THAT THEY WOULD STILL BE BLOCKED BY THE CLOCKING RING.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7138254 ↗
Other ORTHOPEDIC MANUAL SURGICAL INSTRUMENT devices
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- NA 03.010.523Synthes GmbH · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1,208 reports
- EXPRESSEW 214141Medos International Sàrl · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1,166 reports
- N/A 9560524Medtronic Sofamor Danek, Inc. · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT866 reports
- INHANCE 6500-11-104Depuy (Ireland) · Orthopedic manual surgical instrument831 reports
- INHANCE 6500-11-102Depuy (Ireland) · Orthopedic manual surgical instrument567 reports
- R3 71364450Smith & Nephew, Inc. · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT520 reports
- N/A 9561524Medtronic Sofamor Danek, Inc. · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT494 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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