🔍 RecallPedia

QuickGraft¿ Model # 430PST

Class I - Dangerous
🏥 Medical Devices Recalled: August 15, 2019 Musculoskeletal Transplant Foundation Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    Serial # 00319004921075 00319004921073 00319007681048 00319014411085 00618052231059 03319006511040 03319009191029 03319019231072 03519018121056
  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:
Musculoskeletal Transplant Foundation, Inc.
Reason for Recall:
Measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

QuickGraft¿ Model # 430PST

Product Codes/Lot Numbers:

Serial # 00319004921075 00319004921073 00319007681048 00319014411085 00618052231059 03319006511040 03319009191029 03319019231072 03519018121056

Distribution:

Distributed in: NY, NC, LA, TX, MO, OH

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2548-2019

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