# FDA recall Z-2531-2020

> **Philips North  America, LLC** · Class II · device recall initiated 2020-06-08.

## Product

Philips M3015A  Microstream CO2 Extension Model No. 862393 -used with an lntelliVue X3 Patient Monitor (Model No. 867030) or a lntelliVue MMX Multi-Measurement Module (Model No. 867036)

## Reason for recall

Affected M3015A extensions are incompatible with the lntelliVue X3 Patient Monitor (Model No. 867030) and lntelliVue MMX multi-measurement server (Model No. 867036).If they are connected to a host monitor, communication with the X3 or MMX could be disrupted, resulting in a loss of monitoring on the host monitor.

## Distribution

Nationwide  Foreign:  Angola  Angola  Argentina  Australia  Austria  Bahrain  Belarus  Belgium  Bolivia  Brazil  Bulgaria  Canada  Chile  China  Colombia  Costa Rica  Croatia  Cyprus  Czech Republic  Denmark  Egypt  Estonia  Finland  France  French Guiana  Germany  Ghana  Gibraltar  Greece  Greenland  Guadeloupe  Guatemala  Hong Kong  Hungary  Iceland  India  Indonesia  Iran  Ireland  Israel  Italy  Japan  Jordan  Kazakhstan  Kenya  Korea, Republic of  Kuwait  Latvia  Lebanon  Lithuania  Luxembourg  Malaysia  Martinique  Mexico  Morocco  Mozambique  Namibia  Netherlands  New Caledonia  New Zealand  Nicaragua  Norway  Oman  Palestine, State of  Paraguay  Peru  Philippines  Poland  Portugal  Qatar  R¿union  Russian Federation  Saint Pierre and Miquelon  Saudi Arabia  Singapore  Slovakia  Slovenia  South Africa  Spain  Sri Lanka  Sweden  Switzerland  Syrian Arab Republic  Taiwan  Tanzania  Thailand  Turkey  Ukraine  United Arab Emirates  United Kingdom

## Key facts

- **Recall number:** Z-2531-2020
- **Recalling firm:** Philips North  America, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-06-08
- **Report date:** 2020-07-15
- **Termination date:** 2023-01-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Andover, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2531-2020

## Citation

> AI Analytics. FDA recall Z-2531-2020. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-2531-2020. Source: US FDA. Licensed CC0.

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