Respironics RP-UI Assy recall
Respironics RP-UI Assy, V60 Ventilators User Interface RP-Kits, REF/P/N: 453561528931, 453561528941, 453561536451, 453561536461
Why was Respironics RP-UI Assy recalled?
Ventilator touchscreen may become frozen and fail to respond to touch commands. If a patient requires a change in therapy, there is no warning associated with an unresponsive touchcreen, and therefore the clinician would have no prior indication of a touchscreen failure and would be unable to change ventilator settings. The ventilator will continue to function at the predetermined and accepted settings required to support the patient. A delay in therapy adjustments may result in hypercarbia and/or hypoxemia.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
Serial Numbers: 100270400, 100270407, 100256220, 100270404, 100263004, 100266507, 100270402, 100263001, 100263009, 100258193, 100258197, 100258883, 100262978, 100263006, 100258196, 100256196, 100256197, 100256198, 100263003, 100266499, 100266505, 100258889, 100256192, 100258887, 100266509, 100270408, 100262976, 100258881, 100258880, 100266511, 100270406, 100258885, 100256223, 100263000, 100258884, 100258888, 100266500, 100266504, 100258886, 100256222, 100256195, 100256199, 100266502, 100266508, 100266510, 100270403, 100270490, 100257708, 100257713, 100257716, 100256831, 100256834, 100256837, 100262373, 100262556, 100262575, 100265136
- Product
- Respironics RP-UI Assy, V60 Ventilators User Interface RP-Kits, REF/P/N: 453561528931, 453561528941, 453561536451, 453561536461
- Recalling firm
- Respironics California, LLC
- Quantity
- 56
- Distribution
- US Nationwide. OUS (Foreign): Australia, Austria, Bahrain, Belgium, Brazil, Canada, Chile, China, Colombia, Croatia, Finland, France, Germany, Greece, Hong Kong, Iceland, India, Indonesia, Israel, Italy, Malaysia, Mexico, Netherlands, Portugal, Singapore, South Africa, Spain, Sweden, United Arab Emirates, United Kingdom, Viet Nam, Oman, Philippines, Saudi Arabia, Taiwan, Turkey, Russian Federation, Argentina, Ecuador, Poland, Guatemala, Peru, Viet Nam
- Recall date
- February 19, 2020
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)