🔍 RecallPedia

Kit, Port Access Product Code: DYNDC1582A

Class I - Dangerous
🏥 Medical Devices Recalled: July 15, 2019 Centurion Medical Products Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    Lot Number Expiration 2018121350 8/31/2020 2019020750 9/30/2020 2019031550 4/30/2021 2019041550 4/30/2021 2019061750 1/31/2021 2019062450 4/30/2021
  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:
Centurion Medical Products Corporation
Reason for Recall:
Supplier initiated recall of the GRIPPER Needles
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Kit, Port Access Product Code: DYNDC1582A

Product Codes/Lot Numbers:

Lot Number Expiration 2018121350 8/31/2020 2019020750 9/30/2020 2019031550 4/30/2021 2019041550 4/30/2021 2019061750 1/31/2021 2019062450 4/30/2021

Distribution:

Distributed in: IL

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0255-2020

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