🔍 RecallPedia

LITe Decompression Snake Arm, REF 48080230

Class I - Dangerous
🏥 Medical Devices Recalled: November 1, 2023 Stryker Spine Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    UDI-DI (GTIN): 07613327263909, lot # 227764.
  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:
Stryker Spine
Reason for Recall:
Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

LITe Decompression Snake Arm, REF 48080230

Product Codes/Lot Numbers:

UDI-DI (GTIN): 07613327263909, lot # 227764.

Distribution:

Distributed in: US, MD, MI, NM, TX

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0610-2024

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