Magnolia Medical Technologies, Inc.: Medical Device Recall in 2021 - (Recall #: Z-2393-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: August 2, 2021

Date Posted: September 8, 2021

Recall Number: Z-2393-2021

Event ID: 88338

Reason for Recall:

Product was shipped with the incorrect Transfer Adapter Instructions For Use (IFU).

Status: Terminated

Product Quantity: 9,400 units

Code Information:

Catalog #: 27BD-EN, Part #: P00165-000 Lot #9448037

Distribution Pattern:

U.S. Nationwide distribution i the states of AL, CO, FL, GA, IL, IN, MD, MI, NE, NY, PA, SC, TX, VA, WV, and WY. O.U.S.: N/A

Voluntary or Mandated:

Voluntary: Firm initiated