🔍 RecallPedia

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

Class I - Dangerous
🏥 Medical Devices Recalled: August 6, 2025 SEASPINE ORTHOPEDICS Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI-DI: 10889981290733, 10889981437800. Lots: BT107376C, BT112289C, BT112779C, BT107376CR1, BT107376CR2, BT107376CR1R2, BT112289CR2, BT112779CR2
  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:
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.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

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

Product Codes/Lot Numbers:

UDI-DI: 10889981290733, 10889981437800. Lots: BT107376C, BT112289C, BT112779C, BT107376CR1, BT107376CR2, BT107376CR1R2, BT112289CR2, BT112779CR2

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2554-2025

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