Stryker Medical Division of Stryker Corporation: Medical Device Recall in 2021 - (Recall #: Z-2206-2021)

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:

Surgistool-intended to support a healthcare professional during surgical procedures Model 830, Part Number 0830000000

Product Classification:

Class II

Date Initiated: May 12, 2021

Date Posted: August 18, 2021

Recall Number: Z-2206-2021

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: 4 units

Code Information:

Serial Numbers: 1202033898 1206032470 1406034563 1607037109 UDI (DI#): 07613327282566

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