SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to transfer blood between a patient… Recall
Issued September 25, 2024 · B Braun Medical Inc
In September 2024, B Braun Medical Inc recalled the SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to transfer blood between a patient…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Incomplete insertion of the patient connector of the Streamline Airless System Hemodialysis Bloodline to the Locksite may result in the potential for occlusion during prograde rinseback procedures. If the patient connector is not fully inserted into the Locksite, the internal septum may not open fully enough to prevent restrictions to flow. may cause delays in therapy while clinicians are forced to switch to retrograde flow method
What you should do
- 1 Stop using SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to transfer blood between a patient… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact B Braun Medical Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Recall details
- Brand
- B Braun Medical Inc
- Category
- Health
- Recall date
- September 25, 2024
- Units affected
- Not reported
- Sold at
- US Nationwide distribution.
- Recall number
- FDA-Z-3173-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- B Braun Medical Inc has 23 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.