Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

SRHS DeRoyal Heart Tracecart REF 53-1913 Recalled by DeRoyal Industries Inc Due to DeRoyal manufactured custom tracecarts containing a sterile Maquet...

Date: January 25, 2017
Company: DeRoyal Industries Inc
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact DeRoyal Industries Inc directly.

Affected Products

SRHS DeRoyal Heart Tracecart REF 53-1913, Rx Only, NON-STERILE PRODUCT CONTAINED WITHIN.

Quantity: 1157 units

Why Was This Recalled?

DeRoyal manufactured custom tracecarts containing a sterile Maquet Getinge Group chest drainage product which was subsequently recalled due to the current packaging configuration of the Atrium Ocean, Oasis, Express and Express Mini chest drainage products.

Where Was This Sold?

This product was distributed to 2 states: LA, MS

Affected (2 states)Not affected

About DeRoyal Industries Inc

DeRoyal Industries Inc has 225 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report