BD Connecta Stopcock Without Extension Tube Catalog No. 394600 (OUS)

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    GTIN: 382903946006 Lot Numbers/Exp. Date: 1126369 4/30/2024 1126368 4/30/2024 1152277 5/31/2024 1126371 4/30/2024 1152275 5/31/2024 1126366 4/30/2024 1124513 4/30/2024 1126361 4/30/2024 1214381 7/31/2024 1123653 4/30/2024 1123644 4/30/2024 1098342 3/31/2024 1098335 3/31/2024 1098339 3/31/2024 1085949 2/29/2024 1098333 3/31/2024 1090036 2/29/2024 1085634 2/29/2024 1085635 2/29/2024 1090038 2/29/2024 1090820 2/29/2024 1083414 2/29/2024 1063420 2/29/2024 1063419 2/29/2024 1063417 2/29/2024 1060787 2/29/2024 1060784 2/29/2024 1033322 1/30/2024 1060783 2/29/2024 1060791 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. 394600 (OUS)

Product Codes/Lot Numbers:

GTIN: 382903946006 Lot Numbers/Exp. Date: 1126369 4/30/2024 1126368 4/30/2024 1152277 5/31/2024 1126371 4/30/2024 1152275 5/31/2024 1126366 4/30/2024 1124513 4/30/2024 1126361 4/30/2024 1214381 7/31/2024 1123653 4/30/2024 1123644 4/30/2024 1098342 3/31/2024 1098335 3/31/2024 1098339 3/31/2024 1085949 2/29/2024 1098333 3/31/2024 1090036 2/29/2024 1085634 2/29/2024 1085635 2/29/2024 1090038 2/29/2024 1090820 2/29/2024 1083414 2/29/2024 1063420 2/29/2024 1063419 2/29/2024 1063417 2/29/2024 1060787 2/29/2024 1060784 2/29/2024 1033322 1/30/2024 1060783 2/29/2024 1060791 2/29/2024

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1432-2022

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This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.

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