BlossomRecalls & reported problems across all models
Intra-Lock International, Inc. · 66 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 316
- Deaths reported
- 0
- Injuries reported
- 316
- Recalls
- 0
We found 66 models of Blossom by Intra-Lock International, Inc. in the FDA's device registry (GUDID). Together they are named in 316 adverse event reports in the FDA's MAUDE database, received between Feb 24, 2024 and Jun 3, 2026 — classified as 316 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (313 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Blossom problems
Device problems
- Failure to Osseointegrate313
- Use of Device Problem5
- Loss of Osseointegration1
Patient problems
- Insufficient Information316
Blossom models
66 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Blossom S4708Implant, Endosseous, Root-Form24 reports
- Blossom S6006Implant, Endosseous, Root-Form20 reports
- Blossom S4706Implant, Endosseous, Root-Form14 reports
- Blossom SCT4010Implant, Endosseous, Root-Form14 reports
- Blossom SCT4710Implant, Endosseous, Root-Form14 reports
- Blossom S4006Implant, Endosseous, Root-Form11 reports
- Blossom S3708Implant, Endosseous, Root-Form10 reports
- Blossom S4010Implant, Endosseous, Root-Form10 reports
- Blossom S3411Implant, Endosseous, Root-Form9 reports
- Blossom S4015Implant, Endosseous, Root-Form9 reports
- Blossom IS3410TIImplant, Endosseous, Root-Form8 reports
- Blossom SCT4013Implant, Endosseous, Root-Form8 reports
- Blossom IS3710TIImplant, Endosseous, Root-Form7 reports
- Blossom S3413Implant, Endosseous, Root-Form7 reports
- Blossom S3710Implant, Endosseous, Root-Form7 reports
- Blossom S4013Implant, Endosseous, Root-Form7 reports
- Blossom S6008Implant, Endosseous, Root-Form7 reports
- Blossom SCT4711Implant, Endosseous, Root-Form7 reports
- Blossom S3410Implant, Endosseous, Root-Form6 reports
- Blossom S3711Implant, Endosseous, Root-Form6 reports
- Blossom S4008Implant, Endosseous, Root-Form6 reports
- Blossom S3408Implant, Endosseous, Root-Form5 reports
- Blossom S3713Implant, Endosseous, Root-Form5 reports
- Blossom S4011Implant, Endosseous, Root-Form5 reports
- Blossom SCT4010Implant, Endosseous, Root-Form5 reports
- Blossom DT4008STIImplant, Endosseous, Root-Form4 reports
- Blossom S3410Implant, Endosseous, Root-Form4 reports
- Blossom S3710Implant, Endosseous, Root-Form4 reports
- Blossom SCT4011Implant, Endosseous, Root-Form4 reports
- Blossom SCT4710Implant, Endosseous, Root-Form4 reports
- Blossom SCT4713Implant, Endosseous, Root-Form4 reports
- Blossom IS3408TIImplant, Endosseous, Root-Form3 reports
- Blossom S3411Implant, Endosseous, Root-Form3 reports
- Blossom S4011Implant, Endosseous, Root-Form3 reports
- Blossom SCT4711Implant, Endosseous, Root-Form3 reports
- Blossom BLCT4010SImplant, Endosseous, Root-Form2 reports
- Blossom BLCT4011SImplant, Endosseous, Root-Form2 reports
- Blossom BLCT4013SImplant, Endosseous, Root-Form2 reports
- Blossom DT4008STIImplant, Endosseous, Root-Form2 reports
- Blossom DT4011STIImplant, Endosseous, Root-Form2 reports
- Blossom I4711STIImplant, Endosseous, Root-Form2 reports
- Blossom I4713STIImplant, Endosseous, Root-Form2 reports
- Blossom IS3408TIImplant, Endosseous, Root-Form2 reports
- Blossom IS3413TIImplant, Endosseous, Root-Form2 reports
- Blossom IS3710LImplant, Endosseous, Root-Form2 reports
- Blossom IS3710TIImplant, Endosseous, Root-Form2 reports
- Blossom S3708Implant, Endosseous, Root-Form2 reports
- Blossom S3711Implant, Endosseous, Root-Form2 reports
- Blossom S4008Implant, Endosseous, Root-Form2 reports
- Blossom S4013Implant, Endosseous, Root-Form2 reports
- Blossom S6010Implant, Endosseous, Root-Form2 reports
- Blossom SCT4011Implant, Endosseous, Root-Form2 reports
- Blossom SCT4013Implant, Endosseous, Root-Form2 reports
- Blossom BL4010STIImplant, Endosseous, Root-Form1 report
- Blossom BL4011STIImplant, Endosseous, Root-Form1 report
- Blossom DT4010STIImplant, Endosseous, Root-Form1 report
- Blossom DT4010STIImplant, Endosseous, Root-Form1 report
- Blossom DT4010TIImplant, Endosseous, Root-Form1 report
- Blossom I4708STIImplant, Endosseous, Root-Form1 report
- Blossom I4708STIImplant, Endosseous, Root-Form1 report
- Blossom I4710STIImplant, Endosseous, Root-Form1 report
- Blossom I6006STIImplant, Endosseous, Root-Form1 report
- Blossom I6008STIImplant, Endosseous, Root-Form1 report
- Blossom IS3411TIImplant, Endosseous, Root-Form1 report
- Blossom SCT4015Implant, Endosseous, Root-Form1 report
- Blossom SCT4015Implant, Endosseous, Root-Form1 report
Recent Blossom adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 2, 2026Failure to Osseointegrate
InjuryJun 2, 2026Failure to Osseointegrate
InjuryJun 2, 2026Failure to Osseointegrate
InjuryApr 2, 2026Failure to Osseointegrate
InjuryApr 1, 2026Use of Device Problem; Failure to Osseointegrate
InjuryApr 1, 2026Failure to Osseointegrate
InjuryFeb 26, 2026Failure to Osseointegrate
InjuryFeb 26, 2026Failure to Osseointegrate
InjuryFeb 26, 2026Failure to Osseointegrate
InjuryFeb 26, 2026Failure to Osseointegrate
InjuryFeb 26, 2026Failure to Osseointegrate
InjuryFeb 26, 2026Failure to Osseointegrate
InjuryFeb 26, 2026Failure to Osseointegrate
InjuryFeb 26, 2026Failure to Osseointegrate
Other Intra-Lock International, Inc. products
All Intra-Lock International, Inc. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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