Reported Nov 20, 2024 · Ongoing

Philips Zenition 70, Model Number: 718133

Philips Medical Systems Nederland B.v.

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 MEDICAL SYSTEMS NEDERLAND B.V. · Veenpluis 4-6 · Best, N/A · N/A

Is this the product you have?

  • Philips Zenition 70
  • Model Number718133
Lot codes and dates
  • Model Number718133
  • UDI-DI(01)00884838091528(21)
  • Serial Numbers

    2,313 of 2,313 codes

    • 420
    • 4093
    • 2851
    • 3947
    • 2571
    • 4211
    • 3325
    • 3326
    • 2324
    • 3665
    • 491
    • 480
    • 579
    • 580
    • 581
    • 582
    • 4138
    • 71
    • 3657
    • 3660
    • 3889
    • 669
    • 670
    • 671
    • 233
    • 3416
    • 4351
    • 4352
    • 4353
    • 4355
    • 3971
    • 3972
    • 4387
    • 4278
    • 2880
    • 3366
    • 4062
    • 4063
    • 3374
    • 4201
    • 4083
    • 1290
    • 3894
    • 932
    • 933
    • 4309
    • 1796
    • 3355
    • 3680
    • 4156
    • 562
    • 1983
    • 4206
    • 3395
    • 1310
    • 3758
    • 63
    • 1787
    • 2888
    • 684
Amount recalled
2,247 units (582 US, 84 Canada, 1,581 R.O.W.)

This recall covers 2 products

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

Where it was sold

  • Nationwide

Why it was recalled

Potential for the Mains Control Unit board fuse may blow out during system start-up or during a procedure.

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.