Stryker Medical Division of Stryker Corporation: Medical Device Recall in 2023 - (Recall #: Z-1256-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001

Product Classification:

Class II

Date Initiated: February 1, 2023

Date Posted: March 22, 2023

Recall Number: Z-1256-2023

Event ID: 91716

Reason for Recall:

Transport Cot has insufficient volume of epoxy to assemblies installed in the head section and foot sectioning system may result in separation of head end or foot end from the cot and result in unexpected disengagement while loading/unloading or transport.

Status: Ongoing

Product Quantity: 4 units

Code Information:

GTIN: 07613327559118 Serial Numbers: 2208002066, 2208002071, 2209001508, 2208001664

Distribution Pattern:

US Nationwide distribution in the states of NY, VA.

Voluntary or Mandated:

Voluntary: Firm initiated