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FDA (Device enforcement)Recalled 2021-05-12class ii

Stryker Medical Division of Stryker Corporation: Transport Stretcher 747 - a non-powered, wheeled device designed to support patients in a horizontal position, Part Number 0747000000

Is my product affected?

Transport Stretcher 747 - a non-powered, wheeled device designed to support patients in a horizontal position, Part Number 0747000000

  • UPC 07613327278187

Check against the official notice below — it lists the full affected range.

What happened

Stryker Corporation is recalling the Transport Stretcher 747, a wheeled device designed to support patients lying flat. The recall affects 3 units that were distributed to residential customers instead of healthcare facilities. Although the product's labeling correctly identifies that it is intended for use in healthcare settings, home users may not be aware of or fully understand the instructions written for healthcare professionals.

The affected stretchers were distributed worldwide, including across the United States and in Argentina, Brazil, Canada, Chile, Colombia, India, Mexico, and Thailand. The record does not specify a remedy or action that affected consumers should take.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

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

Details from the source

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 Distribution: Worldwide distribution - US Nationwide distribution and the countries of Argentina, Brazil, Canada, Chile, Colombia, India, Mexico, Thailand. Quantity: 3 units Lot/code info: UDI (DI#): 07613327278187

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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