Cardinal Health 200, LLC: Medical Device Recall in 2020 - (Recall #: Z-3016-2020)

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:

KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal S. aureus.

Product Classification:

Class II

Date Initiated: July 30, 2020

Date Posted: October 7, 2020

Recall Number: Z-3016-2020

Event ID: 86178

Reason for Recall:

Only providing one nasal swab in our pre-operative kit instead of the 4 required for proper treatment.

Status: Terminated

Product Quantity: 9,150 kits

Code Information:

Model: ORPDH5994A Lot numbers: 558357, 561502,566549, 571467, 574058. Expiration dates: Varies by kit components.

Distribution Pattern:

US Nationwide distribution including the state of North Carolina.

Voluntary or Mandated:

Voluntary: Firm initiated