🔍 RecallPedia

EIT CIF cage, H 7mm, 8degree, S- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion in patients with cervical disc disease (DDD) Part Number: CUI8070S

Class I - Dangerous
🏥 Medical Devices Recalled: May 20, 2022 DePuy Spine Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI-DI: 04260557770573 Lot Number: E20CL0637
  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:
DePuy Spine, Inc.
Reason for Recall:
Label on the Outer Carton does not match the labels on the Outer Blister package, Inner Blister package and Patient Labels. The only label that may not be correct is on the Outer Carton
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

EIT CIF cage, H 7mm, 8degree, S- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion in patients with cervical disc disease (DDD) Part Number: CUI8070S

Product Codes/Lot Numbers:

UDI-DI: 04260557770573 Lot Number: E20CL0637

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1324-2022

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