Recall Z-2244-2020— Philips North America, LLC

Name: FDA recall Z-2244-2020
Creator: U.S. Food and Drug Administration
Published: 2020-04-13

Class II · Terminated

Class II FDA medical device recall by Philips North America, LLC, initiated 2020-04-13, terminated 2023-04-14. It names one FDA 510(k) clearance: K090785. Product: Cardiovascular Monitoring Device accessory - Product Usage: The chest pneumograph (also referred to as the pneumatic bellows, respiration bellows, or respiration sensor) monitors bellows-derived respiration by detecting abdominal or chest wall motion. The chest pneumograph is an accessory to a MRI patient monitoring system or MRI gating solution. The Chest Pneumograph is indicated for use by healthcare professionals with the Wireless Sp02 (wSp02) Module or Toshiba KSB gating unit when bellows-derived respiration sensing is needed during MRI scans for gating.. Reason: The labeling of the Philips Chest Pneumograph does not include a statement indicating that the product contains natural rubber latex..

Recalling firm: Philips North America, LLC
Classification: Class II
Status: Terminated
Initiated: 2020-04-13
Terminated: 2023-04-14
Firm location: Andover, MA, United States

510(k) clearances named in this recall

1 on FDA's record

K090785 — MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 865214Invivo Corp.·cleared 2009-12-15

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Cardiovascular Monitoring Device accessory - Product Usage: The chest pneumograph (also referred to as the pneumatic bellows, respiration bellows, or respiration sensor) monitors bellows-derived respiration by detecting abdominal or chest wall motion. The chest pneumograph is an accessory to a MRI patient monitoring system or MRI gating solution. The Chest Pneumograph is indicated for use by healthcare professionals with the Wireless Sp02 (wSp02) Module or Toshiba KSB gating unit when bellows-derived respiration sensing is needed during MRI scans for gating.

Reason for recall

The labeling of the Philips Chest Pneumograph does not include a statement indicating that the product contains natural rubber latex.

Data sourced from openFDA. This site is unofficial and independent of the FDA.