White Bronchial Double Lumen Tube Set (Right) Sterile

Class I - Dangerous
🏥 Medical Devices Recalled: November 21, 2014 Teleflex Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Product Code 116201-000350 Batch Number 13FT17, 13GT05, 13GT24, 13HT07, 13HT12, 13HT17, 13IT16, 13IT20, 13JT20, 13JT21, 13JT25R, 13KT05, 13KT05R, 13KT12, 13KT23, 13LT08, 14CT06, 14CT11, 14CT20, 14DT03, 14DT06, 14DT19, 14ET10, 14ET23, 14ET28, 14FT04, 14FT05, 14FT13, 14FT16, 14GT18, 14GT21, 14HT03, 14HT17, 14HT24, 14IT08, 14JT14, 14JT21; Product Code 116201-000370 Batch Number 13FT06, 13GT11, 13GT29, 13HT12, 13HT17, 13IT10, 13IT16, 13IT20R, 13JT08, 13JT20, 13JT25, 13KT05, 13KT12, 13KT23, 13LT08, 13LT11, 14AT08, 14CT06, 14CT11, 14CT20, 14DT19, 14DT24, 14ET04, 14ET10, 14ET22, 14ET23, 14FT04, 14FT13, 14GT18, 14GT21, 14HT03, 14HT20, 14HT23, 14IT05, 14IT08, 14JT14, 14JT18; Product Code 116201-000390 Batch Number 13FT06, 13GT11, 13HT07, 13HT12, 13IT10, 13IT16, 13IT20, 13IT20R, 13JT08, 13JT08R, 13JT20, 13JT21, 13KT12, 13KT18, 14BT16, 14CT06, 14CT16, 14CT20, 14DT03, 14DT13, 14DT24, 14ET10, 14ET23, 14ET28, 14FT13, 14FT16, 14GT05, 14GT18, 14GT21, 14HT03, 14HT09, 14HT20, 14HT23, 14IT08, 14IT14; Product Code 116201-000410 Batch Number 13IT20, 13JT25R, 13KT05R, 13KT12, 13KT15, 13KT18, 13LT11, 14AT08, 14CT11, 14CT16, 14CT21, 14DT13, 14DT19, 14ET04, 14ET22, 14ET28, 14GT18, 14HT03, 14HT17, 14JT12
  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:
Teleflex, Inc.
Reason for Recall:
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

White Bronchial Double Lumen Tube Set (Right) Sterile

Product Codes/Lot Numbers:

Product Code 116201-000350 Batch Number 13FT17, 13GT05, 13GT24, 13HT07, 13HT12, 13HT17, 13IT16, 13IT20, 13JT20, 13JT21, 13JT25R, 13KT05, 13KT05R, 13KT12, 13KT23, 13LT08, 14CT06, 14CT11, 14CT20, 14DT03, 14DT06, 14DT19, 14ET10, 14ET23, 14ET28, 14FT04, 14FT05, 14FT13, 14FT16, 14GT18, 14GT21, 14HT03, 14HT17, 14HT24, 14IT08, 14JT14, 14JT21; Product Code 116201-000370 Batch Number 13FT06, 13GT11, 13GT29, 13HT12, 13HT17, 13IT10, 13IT16, 13IT20R, 13JT08, 13JT20, 13JT25, 13KT05, 13KT12, 13KT23, 13LT08, 13LT11, 14AT08, 14CT06, 14CT11, 14CT20, 14DT19, 14DT24, 14ET04, 14ET10, 14ET22, 14ET23, 14FT04, 14FT13, 14GT18, 14GT21, 14HT03, 14HT20, 14HT23, 14IT05, 14IT08, 14JT14, 14JT18; Product Code 116201-000390 Batch Number 13FT06, 13GT11, 13HT07, 13HT12, 13IT10, 13IT16, 13IT20, 13IT20R, 13JT08, 13JT08R, 13JT20, 13JT21, 13KT12, 13KT18, 14BT16, 14CT06, 14CT16, 14CT20, 14DT03, 14DT13, 14DT24, 14ET10, 14ET23, 14ET28, 14FT13, 14FT16, 14GT05, 14GT18, 14GT21, 14HT03, 14HT09, 14HT20, 14HT23, 14IT08, 14IT14; Product Code 116201-000410 Batch Number 13IT20, 13JT25R, 13KT05R, 13KT12, 13KT15, 13KT18, 13LT11, 14AT08, 14CT11, 14CT16, 14CT21, 14DT13, 14DT19, 14ET04, 14ET22, 14ET28, 14GT18, 14HT03, 14HT17, 14JT12

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2414-2015

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