Becton Dickinson & Company: Medical Device Recall in 2020 - (Recall #: Z-2065-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535

Product Classification:

Class II

Date Initiated: April 16, 2020

Date Posted: May 27, 2020

Recall Number: Z-2065-2020

Event ID: 85432

Reason for Recall:

This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field.

Status: Terminated

Product Quantity: 16,099,310 units

Code Information:

Lots 8353952 9011582 9017875 9024676 9045702 9060999 9079716 9127571 9143529 9156595 9163601

Distribution Pattern:

Nationwide domestic distribution. Foreign distribution to Austria, Belgium, Denmark, Finland, France, Germany, Italy, Netherlands, Norway, Portugal, Spain, Sweden, Switzerland, UK, Australia, Canada, Mexico, Malaysia, New Zealand

Voluntary or Mandated:

Voluntary: Firm initiated