Device recall

Z-2927-2011: Stryker Medical Stretcher Model 1105 Prime 5th Wheel A wheeled stretcher…

FDA device recall · Class II · Stryker Medical Division of Stryker Corporation

Key facts

Recall number (Z-number) Z-2927-2011
Recall event 59214
Product Stryker Medical Stretcher Model 1105 Prime 5th Wheel A wheeled stretcher consists of a platform mounted on a wheeled frame that is designed to transport patients in a horizontal position. The device has siderails and supports for fluid infusion equipment.
Product code INK
Recalling firm Stryker Medical Division of Stryker Corporation
Recall class Class II
Status Terminated
Termination date Aug 28, 2013
FEI number 1831750

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

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