Recall Z-0941-2020— B. Braun Medical, Inc.
Class II · Terminated
Class II FDA medical device recall by B. Braun Medical, Inc., initiated 2019-11-20, terminated 2020-10-16. FDA's recall record names no specific 510(k) clearance for this event. Product: Safeline Y-Type Blood Set, Catalog Number V2500. Reason: Potential for leakage at the joint between the blood filters and tubing.
- Recalling firm
- B. Braun Medical, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-11-20
- Terminated
- 2020-10-16
- Firm location
- Allentown, PA, United States
Product description
Safeline Y-Type Blood Set, Catalog Number V2500
Reason for recall
Potential for leakage at the joint between the blood filters and tubing
Data sourced from openFDA. This site is unofficial and independent of the FDA.