Reef TARecalls & reported problems across all models
Seaspine Orthopedics Corporation · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one Reef TA model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 2 models of Reef TA by Seaspine Orthopedics Corporation in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
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
Reef TA recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Aug 6, 2025Open, Classified
Inserter, used as part of a system with an intervertebral body fusion device, may contribute to difficulty disengaging the implant or improper implant positioning, which may may lead to prolonged surgery, intraoperative revision, and may require the use of alternate instrumentation. Devices may also have incorrect UDI-DI marking.
Z-2554-2025 · Root cause: Device Design · names 2 of these models · Recall details · FDA record ↗
Reef TA models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Reef TA TA2-001002Intervertebral fusion device with bone graft, lumbar1 recall0 reports
- Reef TA TA2-001003Intervertebral fusion device with bone graft, lumbar1 recall0 reports
Other Seaspine Orthopedics Corporation products
- Mariner15 models · 147 reports · 1 recall
- Daytona Small Stature3 models · 14 reports · 2 recalls
- Fathom3 models · 2 reports · 2 recalls
- NorthStar24 models · 15 reports · 1 recall
- Meridian8 models · 8 reports · 1 recall
- Mariner Deformity3 models · 2 reports · 1 recall
- Virata25 models · 0 reports · 1 recall
- Mariner RDX6 models · 0 reports · 1 recall
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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