Becton Dickinson & Company: Medical Device Recall in 2020 - (Recall #: Z-1946-2020)

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:

PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D

Product Classification:

Class II

Date Initiated: March 17, 2020

Date Posted: May 20, 2020

Recall Number: Z-1946-2020

Event ID: 85287

Reason for Recall:

Iincorrectly packaged without the required lidocaine as labeled

Status: Terminated

Product Quantity: 655 kits

Code Information:

Lot Number: REDW0476 20 Exp. Date: 20OCT30 UDI: (01)00801741139390

Distribution Pattern:

AZ, CT, GA, IL, LA, MA, MI, MN, ND, NE, NY, OH, SD, TX),

Voluntary or Mandated:

Voluntary: Firm initiated