BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS)

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    GTIN: 382903946051 Lot Numbers/Exp.Date: 1133181 4/30/2024 1117434 3/31/2024 1110835 3/31/2024 1119671 3/31/2024 1098353 3/31/2024 1098351 3/31/2024 1098350 3/31/2024 1110839 3/31/2024 1110842 3/31/2024 1067265 2/29/2024 1067268 2/29/2024 1067274 2/29/2024 1063372 2/29/2024 1067273 2/29/2024 1067264 2/29/2024 1034587 1/31/2024 1040899 1/31/2024 1034590 1/31/2024 1034594 1/31/2024 1040902 1/31/2024 1040891 1/31/2024 1034597 1/31/2024 1060806 2/29/2024
  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:
Becton Dickinson & Company
Reason for Recall:
May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous material, under dosing/under infusion, contamination and/or air ingress.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS)

Product Codes/Lot Numbers:

GTIN: 382903946051 Lot Numbers/Exp.Date: 1133181 4/30/2024 1117434 3/31/2024 1110835 3/31/2024 1119671 3/31/2024 1098353 3/31/2024 1098351 3/31/2024 1098350 3/31/2024 1110839 3/31/2024 1110842 3/31/2024 1067265 2/29/2024 1067268 2/29/2024 1067274 2/29/2024 1063372 2/29/2024 1067273 2/29/2024 1067264 2/29/2024 1034587 1/31/2024 1040899 1/31/2024 1034590 1/31/2024 1034594 1/31/2024 1040902 1/31/2024 1040891 1/31/2024 1034597 1/31/2024 1060806 2/29/2024

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1435-2022

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An incorrect stopper was used in nine lots of 10mL BD PosiFlush Normal Saline Flush Syringes with General Pump Compatibility. The use of BD PosiFlush Prefilled Flush Syringes with this stopper causes an increase in injection force, which has the potential to trigger alarms if used with a syringe pump.

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