Filtered Triple-Leg Extension Set - Intravascular recall
Filtered Triple-Leg Extension Set - Intravascular administration set. Product Catalog number: 477034 - Product Usage: The extension set is a sterile…
Why was Filtered Triple-Leg Extension Set - Intravascular recalled?
BBMI has identified through complaints the potential for the extension set to become occluded or unable to prime.
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?
Lot #: 00SL713784, 0061741483, 0061755034, 0061755296
- Product
- Filtered Triple-Leg Extension Set - Intravascular administration set. Product Catalog number: 477034 - Product Usage: The extension set is a sterile…
- Recalling firm
- B. Braun Medical, Inc.
- Quantity
- 1,900 units
- Distribution
- US Nationwide distribution in the states of NC, CA.
- Recall date
- May 5, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)