AMO ADMINISTRATION SET, Article No. 7A3817, REF OM2505191, for ophthalmologic use.
This recall is currently active, issued November 3, 2023. It was issued by B Braun Medical Inc.
- Company
- B Braun Medical Inc
- Recall Initiated
- September 26, 2023
- Posted
- November 3, 2023
- Recall Number
- Z-0130-2024
- Quantity
- 32,000
- Firm Location
- Allentown, PA
- Official Source
- View on FDA website ↗
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.
Distribution
Worldwide distribution - US Nationwide and the countries of Canada and Singapore.
Lot / Code Info
UDI-DI: 4046964183454 Lots 0061747706 0061752064 0061755195 0061790409
Root Cause
Process control
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.