Stryker Medical Division of Stryker Corporation: Medical Device Recall in 2021 - (Recall #: Z-2210-2021)

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:

InTouch 2131-intended to support a human patient in an acute care setting, Model Number: 2131000000, Part #1460000000¿¿¿¿¿¿¿

Product Classification:

Class II

Date Initiated: May 12, 2021

Date Posted: August 18, 2021

Recall Number: Z-2210-2021

Event ID: 88199

Reason for Recall:

Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals

Status: Ongoing

Product Quantity: 2 units

Code Information:

Serial Numbers: U54274 U71491 UDI:07613327169294

Distribution Pattern:

Worldwide distribution - US Nationwide distribution and the countries of Argentina, Brazil, Canada, Chile, Colombia, India, Mexico, Thailand.

Voluntary or Mandated:

Voluntary: Firm initiated