Magnetic Resonance Imaging Diagnostic Device accessory recall: Labeling Error
Magnetic Resonance Imaging Diagnostic Device accessory - Product Usage: The chest pneumograph (also referred to as the pneumatic bellows, respiration…
Why was Magnetic Resonance Imaging Diagnostic Device accessory recalled?
The labeling of the Philips Chest Pneumograph does not include a statement indicating that the product contains natural rubber latex.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Every lot distributed since 1996 with Part #94023
- Product
- Magnetic Resonance Imaging Diagnostic Device accessory - Product Usage: The chest pneumograph (also referred to as the pneumatic bellows, respiration…
- Recalling firm
- Philips North America, LLC
- Quantity
- 1075 Units
- Distribution
- US Nationwide distribution.
- Recall date
- June 10, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)