Reported Nov 29, 2023 · Ongoing

Achieva 1.5T Conversion

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 Conversion
Lot codes and dates
  • Product No. 781283 & 781346
  • UDI-DI

    136 of 136 codes

    • (01)00884838009806(21)39001
    • (01)00884838009806(21)39027
    • (01)00884838009806(21)39028
    • (01)00884838009806(21)39030
    • (01)00884838009806(21)39032
    • (01)00884838009806(21)39039
    • (01)00884838009806(21)39053
    • (01)00884838009806(21)39059
    • (01)00884838009806(21)39061
    • (01)00884838009806(21)39062
    • (01)00884838009806(21)39064
    • (01)00884838009806(21)39065
    • (01)00884838009806(21)39066
    • (01)00884838009806(21)39067
    • (01)00884838009806(21)39072
    • (01)00884838009806(21)39073
    • (01)00884838009806(21)39074
    • (01)00884838009806(21)39075
    • (01)00884838009806(21)39078
    • (01)00884838009806(21)39080
    • (01)00884838009806(21)39081
    • (01)00884838009806(21)39082
    • (01)00884838009806(21)39083
    • (01)00884838009806(21)39084
    • (01)00884838009806(21)39086
    • (01)00884838009806(21)39088
    • (01)00884838009806(21)39090
    • (01)00884838009806(21)39091
    • (01)00884838009806(21)39093
    • (01)00884838009806(21)39094
    • (01)00884838009806(21)39095
    • (01)00884838009806(21)39097
    • (01)00884838009806(21)39098
    • (01)00884838009806(21)39100
    • (01)00884838009806(21)39102
    • (01)00884838009806(21)39105
    • (01)00884838009806(21)39106
    • (01)00884838009806(21)39107
    • (01)00884838068469(21)5243
    • (01)00884838068469(21)5547
    • (01)00884838068469(21)8020
    • (01)00884838068469(21)8276
    • (01)00884838068469(21)8289
    • (01)00884838068469(21)8361
    • (01)00884838068469(21)8367
    • (01)00884838068469(21)8371
    • (01)00884838068469(21)8415
    • (01)00884838068469(21)8714
    • (01)00884838068469(21)8727
    • (01)00884838068469(21)8740
    • (01)00884838068469(21)8782
    • (01)00884838068469(21)10189
    • (01)00884838068469(21)10194
    • (01)00884838068469(21)10219
    • (01)00884838068469(21)10821
    • (01)00884838068469(21)18505
    • (01)00884838068469(21)18737
    • (01)00884838068469(21)75000
    • (01)00884838068469(21)75003
    • (01)00884838068469(21)75004
Amount recalled
68 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, 6:58 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.