FDA Medical Device Recalls (openFDA)
SEASPINE ORTHOPEDICS CORPORATION: 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
- Recall number
- Z-0752-2025
- Recalling firm
- SEASPINE ORTHOPEDICS CORPORATION
- Product
- 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
- Status
- Open, Classified
- Initiated
- 2024-10-29
- Posted
- 2024-12-23
- Terminated
- not on file
- Reason
- Due to manufacturing defects observed on Locking Caps that affect the ability for components to mate.
- Root cause
- Nonconforming Material/Component
- Action
- Update 12/18/2024 - The firm sent an updated Customer Notification Letter on 12/12/2024 to customers that have not responded to the initial notification on 10/29/2024. On 10/29/2024, firm sent an "URGENT: MEDICAL DEVICE RECALL" Letter to customer informing them that the firm has identified a nonconformance with the threads of the locking cap components that may be incongruous with optimal manufacturing specifications. The nonconformance can result in a locking cap that does not mate appropriately with the screw tulip. Customers are instructed to: -Review their inventory and return the affected part(s) using the provided label to return the inventory in their possession. Any questions contact Dalton Daggs at Dalton.daggs@seaspine.com or Danielle Nelson-Archer at Danielle.nelson-archer@seaspine.com.
- Quantity
- 191 devices
- Distribution
- U.S. Nationwide distribution in the states of CA, CO, FL, GA, PA, TX, and VA.
- Lot, serial or model codes
- Lot Code: PN 79-0001 UDI 10889981185633 Lot Numbers MM2098114B
- 510(k) numbers
- ["K232566"]
- PMA numbers
- not on file
- Product code
- NKB
- Firm FEI
- 3012120772
- Firm city
- Carlsbad
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28