Cardinal Health 200, LLC: Medical Device Recall in 2021 - (Recall #: Z-2038-2021)

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:

Nonsterile Femoral Angiography Drape, Catalog Numbers: a) 29460NB, b) 29456NB - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.

Product Classification:

Class II

Date Initiated: May 21, 2021

Date Posted: July 14, 2021

Recall Number: Z-2038-2021

Event ID: 88046

Reason for Recall:

The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.

Status: Terminated

Product Quantity: 15360 units

Code Information:

a) 29460NB: Lot Numbers: 0071PR1, 0121PR1, 0131PR1, 0141PR1, 0271PR1, 0281PR1, 0291PR1, 0351PR1, 0361PR1, 0391PR1, 0401PR1, 3040PR1, 3110PR1, 3250PR1, 3380PR1, 3510PR1, 3520PR1, 3530PR1 b) 29456NB: Lot Numbers: 3290LR1, 3300LR1, 3310LR1, 3320LR1, 3350LR1, 3390LR1, 3420LR1

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated