Integra LifeSciences Corp.: Medical Device Recall in 2022 - (Recall #: Z-0818-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Codman Cranial Access Kits- indicated when a craniotomy is required for placement of an intracranial pressure (ICP) monitoring device and/or cerebrospinal fluid drainage procedures. Part Number: 826616

Product Classification:

Class II

Date Initiated: January 21, 2022

Date Posted: March 30, 2022

Recall Number: Z-0818-2022

Event ID: 89618

Reason for Recall:

Incorrect extended expiration dates identified on the outer box label only, if product is used past the correct expiration date there is a potential for pain, infection, or adverse tissue reaction to occur

Status: Terminated

Product Quantity: 1160 kits

Code Information:

Lot Numbers: 20DDA264, 21HDA861 UDI# 10381780520382

Distribution Pattern:

Worldwide distribution - US Nationwide and the country of Hong Kong.

Voluntary or Mandated:

Voluntary: Firm initiated