B. Braun Medical, Inc. IV Administration Set with Universal Spike, two Ultrasite Injection Sites, Backcheck Valve and Spin-Lock Connector, Catalog # 352049. For use with Secondary Container. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
IV Administration Set with Universal Spike, two Ultrasite Injection Sites, Backcheck Valve and Spin-Lock Connector, Catalog # 352049. For use with Secondary Container.
Brand
B. Braun Medical, Inc.
Lot Codes / Batch Numbers
Catalog #352049 - Lot #'s 61028761, 61028762, 61028763, 61028764, 61028765, 61028766, 61028767, 61028769, 61028771, and 61028772 all with an expiration date of 1/31/2014.
Products Sold
Catalog #352049 - Lot #'s 61028761, 61028762, 61028763, 61028764, 61028765, 61028766, 61028767, 61028769, 61028771, and 61028772 all with an expiration date of 1/31/2014.
B. Braun Medical, Inc. is recalling IV Administration Set with Universal Spike, two Ultrasite Injection Sites, Backcheck Valve and Spin- due to Device defect is occlusion/no flow.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Device defect is occlusion/no flow.
Recommended Action
Per FDA guidance
An Urgent - Medical Device Recall notice was issued via US Postal Service Certified Mail with registered return receipt mail or FedEx to all customer/distributors in receipt of affected product on 3/27/09. Direct customers received letters addressed to Materials Management that informed them of this recall and provided instructions for disposition of affected product in their inventory. Distributors received the direct customer recall letter along with a cover letter outlining their responsibilities to execute the recall and notify their customers as requested. Distributors are to immediately discontinue further distribution of the affected product, determine their customers' inventory, and have their customers return the product to them. The attached "Product Removal Acknowledgement" should be used to indicate the specifics of the combined distributor and customer inventories. The Customer Support Department should be contacted to arrange for return. A Customer Support Representative will provide instructions for handling the affected product and assist with replacement product.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026