FDAApril 13, 2020device

Magnetic Resonance Imaging Diagnostic 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 acces...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Terminated

Brands named

philips north americaphilipsphilips north

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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