Reported Nov 29, 2023 · Ongoing

Achieva 1.5T

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?

  • Achieva 1.5T
Lot codes and dates
    • Product No. 781178
    • 781196
    • 781296
    • & 781343
  • UDI-DI

    917 of 917 codes

    • (01)00884838004108(21)8524
    • (01)00884838004108(21)32039
    • (01)00884838004108(21)32052
    • (01)00884838004108(21)32083
    • (01)00884838004108(21)32087
    • (01)00884838004108(21)32097
    • (01)00884838004108(21)32103
    • (01)00884838004108(21)32118
    • (01)00884838004108(21)32123
    • (01)00884838004108(21)32150
    • (01)00884838004108(21)32153
    • (01)00884838004108(21)32154
    • (01)00884838004108(21)32186
    • (01)00884838004108(21)32223
    • (01)00884838004108(21)32226
    • (01)00884838004108(21)32228
    • (01)00884838004108(21)32230
    • (01)00884838004108(21)32231
    • (01)00884838004108(21)32243
    • (01)00884838004108(21)32247
    • (01)00884838004108(21)32255
    • (01)00884838004108(21)32265
    • (01)00884838004108(21)32288
    • (01)00884838004108(21)32289
    • (01)00884838004108(21)32306
    • (01)00884838004108(21)32350
    • (01)00884838004108(21)32375
    • (01)00884838004108(21)32376
    • (01)00884838004108(21)32385
    • (01)00884838004108(21)32387
    • (01)00884838004108(21)32390
    • (01)00884838004108(21)32392
    • (01)00884838004108(21)32413
    • (01)00884838004108(21)32435
    • (01)00884838004108(21)32439
    • (01)00884838004108(21)32452
    • (01)00884838004108(21)32459
    • (01)00884838004108(21)32463
    • (01)00884838004108(21)32474
    • (01)00884838004108(21)32505
    • (01)00884838004108(21)32531
    • (01)00884838004108(21)32533
    • (01)00884838004108(21)32537
    • (01)00884838004108(21)32567
    • (01)00884838004108(21)32584
    • (01)00884838004108(21)32591
    • (01)00884838004108(21)32595
    • (01)00884838004108(21)32603
    • (01)00884838004108(21)32608
    • (01)00884838004108(21)32610
    • (01)00884838004108(21)32631
    • (01)00884838004108(21)32655
    • (01)00884838004108(21)32675
    • (01)00884838004108(21)32684
    • (01)00884838004108(21)32708
    • (01)00884838004108(21)32720
    • (01)00884838004108(21)32727
    • (01)00884838004108(21)32728
    • (01)00884838004108(21)32739
    • (01)00884838004108(21)32748
Amount recalled
520 units

This recall covers 7 products

The agency filed one notice per product. You are reading one of them; the other 6 are below.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Potential component failure in the Gradient Coil could product smoke and/or fire.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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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, 6:20 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.