Blossom SCT4710 (UDI D742SCT47100)Recalls & reported problems
Intra-Lock International, Inc. · Gw Blossom™ CT Implant Ø4.75 x 10mm + Cover Screw · Class 2 · Implant
All models of Blossom (66)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 14
- Deaths reported
- 0
- Injuries reported
- 14
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI D742SCT47100), received between Feb 24, 2024 and Feb 25, 2026 — classified as 14 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (14 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.
Reports received per month
Most reported problems
Device problems
- Failure to Osseointegrate14
- Loss of Osseointegration1
Patient problems
- Insufficient Information14
Recent adverse event reports
The 14 most recent of 14 reports, in the reporter's own words as published by the FDA.
InjuryFeb 25, 2026Failure to Osseointegrate
InjurySep 19, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 22, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 22, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 27, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 31, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 14, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 14, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 6, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 6, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 5, 2024Failure to Osseointegrate; Loss of Osseointegration; Failure to Osseointegrate; Loss of Osseointegration
InjuryFeb 24, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryFeb 24, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryFeb 24, 2024Failure to Osseointegrate; Failure to Osseointegrate
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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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