Magnolia Medical Technologies, Inc. Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This holder/adapter assembly may be used for the access of a specimen from Catheter Port to BD Vacutainer Blood Collection or Urine Collection Tubes. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This holder/adapter assembly may be used for the access of a specimen from Catheter Port to BD Vacutainer Blood Collection or Urine Collection Tubes.
Brand
Magnolia Medical Technologies, Inc.
Lot Codes / Batch Numbers
Catalog #: 27BD-EN, Part #: P00165-000 Lot #9448037
Products Sold
Catalog #: 27BD-EN, Part #: P00165-000 Lot #9448037
Magnolia Medical Technologies, Inc. is recalling Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This holder/adapter assembly may be u due to Product was shipped with the incorrect Transfer Adapter Instructions For Use (IFU).. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Product was shipped with the incorrect Transfer Adapter Instructions For Use (IFU).
Recommended Action
Per FDA guidance
On or about 08/02/2021, the firm hand delivered via its Clinical Team an "URGENT: MEDICAL DEVICE RECALL" Notification letter to customers informing them that a specific lot number of transfer adapters was shipped with the incorrect Instructions for Use. Customers are instructed to work with the Recalling Firm's Clinical Team member in identifying the affected products so that replacement Instructions for Use can be provided at no cost. Customers are also instructed to complete a Customer Acknowledgement Form, to record the quantity of affected products each customer has in their inventory and return to their local Recalling Firm's Clinical Team member, or directly to the Recalling Firm. For questions or assistance, contact Customer Service and Sales at 415-969-8183 or email kristine.delavega@magnolia-medical.com
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