Daytona CoCr LockingCap 4.5mm: Manufacturing defect affects component mating
SEASPINE ORTHOPEDICS CORPORATION recalls Daytona Small Stature CoCr LockingCap 4:5mm models with manufacturing defects that may prevent proper component mating. Affected units include specific lot numbers and model 79-0002.
Lower-risk recall
Due to manufacturing defects observed on Locking Caps that affect the ability for components to mate.
Contact the company
What happened, in plain English
SEASPINE ORTHOPEDICS CORPORATION is recalling Daytona Small Stature CoCr LockingCap 4.5mm implants due to manufacturing defects that could cause components to not mate properly. This may lead to improper function of the implant. Read more at govinfonow.com/recall/53621-daytona-cocr-lockingcap-4-5mm-manufacturing-defect-affects-component-mating.
Source Summary by GovInfoNow · govinfonow.com/recall/53621-daytona-cocr-lockingcap-4-5mm-manufacturing-defect-affects-component-mating · Updated August 18, 2026 · FDA enforcement record: FDA #Z-0751-2025
Cite this page
“Daytona CoCr LockingCap 4.5mm: Manufacturing defect affects component mating.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/53621-daytona-cocr-lockingcap-4-5mm-manufacturing-defect-affects-component-mating. Based on FDA recall #Z-0751-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0751-2025%22&limit=1).
Why it’s dangerous
The locking caps have manufacturing defects that prevent components from mating correctly. This could lead to improper function of the implant, but the hazard does not involve immediate injury or serious harm in normal use.
Who’s affected
People who own or use Daytona Small Stature CoCr LockingCap 4.5mm implants with model number 79-0002 are affected. Patients with these implants are most at risk.
How to tell if you have this one
Check for model number 79-0002 on the implant. Affected units were sold with lot numbers MM1002742E and MM1003065E.
- Brand
Daytona- Category
Medical device
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
U.S. Nationwide distribution in the states of CA, CO, FL, GA, PA, TX, and VA.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-0751-2025 | Brand Name: Daytona Small Stature Product Name: CoCr LockingCap 4.5mm, Small Stature, T25, BT Model/Catalog Number: 79-0002 Software Version: N/A Product Description: Locking Cap Component: No; Lot Code: PN 79-0002 UDI 10889981185640 Lot Numbers MM1002742E, MM1003065E | 92 devices |
| Z-0752-2025 | Brand Name: Daytona Small Stature Product Name: Ti Locking Cap 4.5mm, Small Stature, T25 Model/Catalog Number: 79-0001 Software Version: N/A Product Description: Locking Cap Component: No; Lot Code: PN 79-0001 UDI 10889981185633 Lot Numbers MM2098114B | 191 devices |
What to do — step by step
Check Model Number
Look for model number 79-0002 on the implant to confirm if it is affected.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 7 states.
FDA distribution: “U.S. Nationwide distribution in the states of CA, CO, FL, GA, PA, TX, and VA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Colorado, Florida, Georgia, Pennsylvania, Texas, Virginia.
Recall timeline
FDA published this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-0751-2025 (October 29, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0751-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.