Bronchial Double Lumen Tube Set recall
Bronchial Double Lumen Tube Set (Left), Extra Length, Sterile
Why was Bronchial Double Lumen Tube Set recalled?
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Product Code 116164-000390 Batch Number 14BT21
- Product
- Bronchial Double Lumen Tube Set (Left), Extra Length, Sterile
- Recalling firm
- Teleflex, Inc.
- Distribution
- AL, AK, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MD, MA, MI, MS, MO, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV. WI, DC, Puerto Rico, Canada, Bolivia, Ecuador, Hong Kong, Malaysia, Philippines, Taiwan, Trinidad & Tobago
- Recall date
- August 26, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)