🔍 RecallPedia

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

Class I - Dangerous
🏥 Medical Devices Recalled: October 29, 2024 SEASPINE ORTHOPEDICS Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Code: PN 79-0002 UDI 10889981185640 Lot Numbers MM1002742E, MM1003065E
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
SEASPINE ORTHOPEDICS CORPORATION
Reason for Recall:
Due to manufacturing defects observed on Locking Caps that affect the ability for components to mate.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

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

Product Codes/Lot Numbers:

Lot Code: PN 79-0002 UDI 10889981185640 Lot Numbers MM1002742E, MM1003065E

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0751-2025

Related Recalls

Reef TA Inserter, Part Number: TA2-001003, part of the Reef Interbody System

SEASPINE ORTHOPEDICS

Class I - Dangerous

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.

Aug 6, 2025 Other Medical Devices Nationwide View Details →