BD MaxGuard Extension Set with 2 Needleless Y-Site, REF: MX9059

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI-DI: 10885403237584, Lots: 22029431, 22029432
  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:
CAREFUSION
Reason for Recall:
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

BD MaxGuard Extension Set with 2 Needleless Y-Site, REF: MX9059

Product Codes/Lot Numbers:

UDI-DI: 10885403237584, Lots: 22029431, 22029432

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1757-2022

Related Recalls

Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

Aug 1, 2022 Surgical Instruments Nationwide View Details →