Integra LifeSciences Corp.: Medical Device Recall in 2022 - (Recall #: Z-0906-2022)

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:

Integra Universal Flexible Arm part number REF 1362275

Product Classification:

Class II

Date Initiated: February 28, 2022

Date Posted: April 20, 2022

Recall Number: Z-0906-2022

Event ID: 89830

Reason for Recall:

Excess force used to tighten the Universal Flexible Arm can cause the internal cable to break at the tip, resulting in an unusable condition.

Status: Ongoing

Product Quantity: 54

Code Information:

UDI#10381780074670, Lots: AC2109, AC2103, AC2106, AC2110, AC2101, AC2008, AC2009

Distribution Pattern:

US Nationwide Distribution: AL, AZ, FL, GA, IL, MA, MD, NY, OH, OR, PA, TX

Voluntary or Mandated:

Voluntary: Firm initiated