Cardinal Health 200, LLC: Medical Device Recall in 2021 - (Recall #: Z-1251-2021)

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:

McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. Product Code: 26558

Product Classification:

Class II

Date Initiated: February 9, 2021

Date Posted: March 24, 2021

Recall Number: Z-1251-2021

Event ID: 87313

Reason for Recall:

Safety shield not locking into the cannula. If the safety shield activation fails to lock a contaminated needle, a needlestick may occur and there is the potential for exposure to bloodborne pathogens

Status: Terminated

Product Quantity: 108,000 units

Code Information:

Lot Code: 028603

Distribution Pattern:

Worldwide distribution - US Nationwide distribution and the countries of AE, Japan.

Voluntary or Mandated:

Voluntary: Firm initiated