Asnis 40-30120Recalls & reported problems
Stryker GmbH · CANNULATED SCREW · Class 2 · Implant
All models of ASNIS (51)
Data updated Oct 18, 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 07613154578047), received between Nov 6, 2025 and Nov 6, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Biocompatibility” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Biocompatibility1
Patient problems
- Erythema1
- Hypersensitivity/Allergic reaction1
- Low Blood Pressure/ Hypotension1
- Nausea1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 6, 2025Biocompatibility; Biocompatibility
IT WAS REPORTED THAT A PATIENT CONTACTED STRYKER TO CONFIRM THE MATERIAL COMPOSITION OF A 20MM PARTIALLY THREADED CANNULATED SCREW. THE PATIENT HAS A KNOWN COBALT ALLERGY AND IS EXPERIENCING LOW BLOOD PRESSURE IN THE EVENINGS, NAUSEA AFTER EATING, AND LOCALIZED REDNESS NEAR THE SURGICAL SITE (WITHOUT SIGNS OF INFECTION). THE PATIENT IS CONSIDERING IMPLANT REMOVAL, BUT INSURANCE WILL ONLY COVER THE REVISION IF COBALT EXPOSURE IS CONFIRMED, SO THEY ARE REQUESTING CLARIFICATION ON WHETHER THE SCREW CONTAINS COBALT OR IS PURE TITANIUM.
Patient problems: Erythema; Hypersensitivity/Allergic reaction; Low Blood Pressure/ Hypotension; Nausea
MAUDE report 23490591 ↗
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- PRECICE® Bone Transport System STP3.5-400Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-225Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-350Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-300Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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