Stryker Corporation: Medical Device Recall in 2024 - (Recall #: Z-2259-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.
Product Description:

The Non-Sterile Flyte hood covers the user s head and neck region and is intended to be worn with commercially available gowns. The hood is donned after the Flyte helmet and before the gown, such that the hood is securely tucked inside the gown. The hood attaches to and covers the helmet and air is drawn into the helmet through a filter located on the top-backside of the hood. The filtered air is delivered into the helmet and the disposable does not inhibit adjustment of helmet settings/functions. Catalog Number: 0408-800-000NS

Product Classification:

Class II

Date Initiated: June 3, 2024
Date Posted: July 10, 2024
Recall Number: Z-2259-2024
Event ID: 94755
Reason for Recall:

Expired Products distributed to customers

Status: Ongoing
Product Quantity: 4 units
Code Information:

GTIN: 07613327514063 Lot Number: 20040649

Distribution Pattern:

US Nationwide distribution in the states of Arkansas, California, Colorado, Florida, Michigan.

Voluntary or Mandated:

Voluntary: Firm initiated