TOETAC HT-00005Recalls & reported problems
Stryker GmbH · Hammertoe Implant, Medium, 10 degree · Class 2 · Implant
Data updated Oct 18, 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 07613327356298), received between Jun 18, 2019 and Jun 18, 2019 — 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 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Erythema2
- Hypersensitivity/Allergic reaction2
- Urticaria1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJun 18, 2019Appropriate Device Problem Term/Code Not Available
IT WAS REPORTED THAT THE PATIENT SEEMS TO HAVE ALLERGIC REACTION TO THE TOE TAC IMPLANTS. REDNESS AND HIVES AROUND THE SITES. PATIENT WAS REVISED.
Patient problems: Erythema; Hypersensitivity/Allergic reaction; Urticaria
MAUDE report 8709880 ↗InjuryJun 18, 2019Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT SEEMS TO HAVE ALLERGIC REACTION TO THE TOE TAC IMPLANTS. REDNESS AND HIVES AROUND THE SITES. PATIENT WAS REVISED.
Patient problems: Erythema; Hypersensitivity/Allergic reaction
MAUDE report 8709879 ↗
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- HEALIX PEEK ORTHOCORD 222205Medos International Sàrl · Screw, fixation, bone186 reports
- 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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