🔍 RecallPedia

Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F, REF 4992209 Version A, Sterile EO, Rx Only

Class I - Dangerous
🏥 Medical Devices Recalled: April 22, 2023 Merit Medical Systems Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot # I2533611, I2546597, I2559292, I2548163 & I2578001; UDI-DI: 00884450394908
  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:
Merit Medical Systems, Inc.
Reason for Recall:
There is a potential that valve assemblies will not open. preventing fluid from draining.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F, REF 4992209 Version A, Sterile EO, Rx Only

Product Codes/Lot Numbers:

Lot # I2533611, I2546597, I2559292, I2548163 & I2578001; UDI-DI: 00884450394908

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1911-2023

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