Stryker Medical Division of Stryker Corporation: Medical Device Recall in 2021 - (Recall #: Z-2207-2021)

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:

Prime Fifth Wheel Stretcher-stretcher may be used for minor procedures and short-term stay (treatment and recovery, Model 1105, Part Numbers 1105000026 and 1105000000X

Product Classification:

Class II

Date Initiated: May 12, 2021

Date Posted: August 18, 2021

Recall Number: Z-2207-2021

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: 3 units

Code Information:

UDI (DI#) 07613327278149 07613327278149 07613327278194

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