SA3000 VENTED MICRO SPIKE ADAPTER, REF No. 418121, for intravenous use.
FDA device recall Z-0129-2024 · posted 2023-11-03 · Open, Classified
Recall details
- Recalling firm
- B. Braun Medical, Inc.
- Reason for recall
- Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and healthcare workers to hazardous medication. There is also the potential for life-threatening situations to occur requiring additional medical intervention.
- Action taken
- On September 26, 2023, the firm notified customers via Urgent Product Recall Notification letters. Customers were informed of the potential for leakage at the male Luer lock site. Customers were instructed to report total amount of impacted product on hand to the firm, after which B Braun Customer Support will contact the customer with instructions on how to return the product for credit or replacement depending on the customer's need. Questions about this recall may be reported to BBMI s Postmarket Surveillance Department by calling 1-833-425-1464.
- Root cause
- Process control
- Status
- Open, Classified
- Product code
- FPA
- Quantity affected
- 17,100 units
- Distribution
- Worldwide distribution - US Nationwide and the countries of Canada and Singapore.
- Date initiated
- 2023-09-26
- Date posted
- 2023-11-03
- Location
- Allentown, PA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| I.V. ADMINISTRATION SET WITH MINI-SPIKE (K780551) | National Patent Development Corp. | 1978-04-19 |