Reported Feb 12, 2025 · Ongoing

IntelliBridge EC10 Module. Model Number: 865115

Philips North America LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Philips North America Llc · 222 Jacobs St · Cambridge, MA · 02141-2289

Is this the product you have?

  • IntelliBridge EC10 Module
  • Model Number865115
Lot codes and dates
  • Model Number865115
  • UDI-DI Number(01)00884838015951(21)
  • Serial Numbers

    2,230 of 2,230 codes

    • DE57029003
    • DE57028993
    • DE57028976
    • DE57028982
    • DE57028983
    • DE57028987
    • DE57028988
    • DE57028951
    • DE57028992
    • DE57029001
    • DE57029002
    • DE57028989
    • DE57028990
    • DE57028991
    • DE57029000
    • DE61951169
    • DE61951170
    • DE61951171
    • DE61951143
    • DE61951141
    • DE61951139
    • DE61951172
    • DE61951173
    • DE61951193
    • DE61951096
    • DE70164542
    • DE70164538
    • DE70164539
    • DE70164540
    • DE70169842
    • DE70169843
    • DE70169846
    • DE70175669
    • DE57034208
    • DE57034005
    • DE57034248
    • DE57034244
    • DE57034243
    • DE57034241
    • DE57034237
    • DE57034234
    • DE57034231
    • DE57034261
    • DE57034245
    • DE57034238
    • DE57034229
    • DE57034220
    • DE57034030
    • DE57034188
    • DE57034679
    • DE57034671
    • DE73784113
    • DE73784325
    • DE73784414
    • DE73784137
    • DE70171598
    • DE70171596
    • DE70171601
    • DE70171602
    • DE70171597
Amount recalled
2,230 units

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

Why it was recalled

Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:56 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.