Becton Dickinson & Company: Medical Device Recall in 2020 - (Recall #: Z-0295-2021)

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:

Bard 3F SL PowerMidline Full Kit CE-indicated for short term access to the peripheral venous system for selected intravenous therapies, blood sampling, and power injection of contrast media Ref: P6153208

Product Classification:

Class II

Date Initiated: September 14, 2020

Date Posted: November 4, 2020

Recall Number: Z-0295-2021

Event ID: 86477

Reason for Recall:

Kits do not contain the stylet/T-lock assembly indicated as a component on the label, may lead to a procedural delay and possibly discard of the kit.

Status: Terminated

Product Quantity: 72 units

Code Information:

Lot Number: REEQ3598 Feb-2022 and REER0518 Mar-2022 UDI: 00801741141065

Distribution Pattern:

Foreign: Italy, Spain, and UK

Voluntary or Mandated:

Voluntary: Firm initiated