Respironics RP-Touch Screen — Class II medical device recall Z-1154-2020
Ongoing recall by Respironics California, LLC, reported 2020-02-19, distributed nationwide. Ventilator touchscreen may become frozen and fail to respond to touch commands. If a patient requires a change
| Recall number | Z-1154-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Respironics California, LLC, Carlsbad, CA, United States |
| Recall initiated | 2019-09-11 |
| Classified | 2020-02-12 |
| Reported by FDA | 2020-02-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BE, BH, BR, CA, CL, CN, CO, DE, EC, ES, FI, FR, GB, GR, GT, HK, HR, ID, IL, IN, IS, IT, MX, MY, NL, OM, PE, PH, PL, PT, SA, SE, SG, TR, TW, VN, ZA |
| Quantity | 800 |
| Serial numbers | 0092, 0107, 0117, 0130, 0134, 0137, 0138, 0140, 0141, 0143, 0146, 0150, 0165, 0175, 0179, 0183, 0195, 0200, 0250, 0275, 0285, 0295, 0328, 41088-1808-0001, 41213-1809-0001 and 22 more |
| Model numbers | 1132318 |
Product
Respironics RP-Touch Screen, V60/V680 Ventilator Serviced with Touchscreen RP Kit 453561511951 containing a touchscreen labeled as raw part number 1132318 Revision C
Reason for recall
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.
Machine access
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Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.