Reported Dec 13, 2023 · Ongoing

DRX Revolution Mobile X-Ray System

Carestream Health, Inc.

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: Carestream Health, Inc. · 1049 W Ridge Rd · Rochester, NY · 14615-2731

Is this the product you have?

  • DRX Revolution Mobile X-Ray System
Lot codes and dates
  • 2,635 of 2,635 codes

    • Catalog No. 1019397
    • 1023423
    • 1030717
    • 1030725
    • 1044726
    • 1060177
    • 8608754
    • 1023415
    • 8610180
    • 8618894
    • UDI-DI (01)60889971019394(21)2185
    • (01)60889971019394(21)2186
    • (01)60889971019394(21)2187
    • (01)60889971019394(21)2193
    • (01)60889971019394(21)2194
    • (01)60889971019394(21)2195
    • (01)60889971019394(21)2196
    • (01)60889971019394(21)2200
    • (01)60889971019394(21)2203
    • (01)60889971019394(21)2204
    • (01)60889971019394(21)2205
    • (01)60889971019394(21)2206
    • (01)60889971019394(21)2207
    • (01)60889971019394(21)2208
    • (01)60889971019394(21)2209
    • (01)60889971019394(21)2210
    • (01)60889971019394(21)2213
    • (01)60889971019394(21)2217
    • (01)60889971019394(21)2218
    • (01)60889971019394(21)2221
    • (01)60889971019394(21)2227
    • (01)60889971019394(21)2232
    • (01)60889971019394(21)2233
    • (01)60889971019394(21)2235
    • (01)60889971019394(21)2236
    • (01)60889971019394(21)2237
    • (01)60889971019394(21)2240
    • (01)60889971019394(21)2243
    • (01)60889971019394(21)2247
    • (01)60889971019394(21)2248
    • (01)60889971019394(21)2249
    • (01)60889971019394(21)2250
    • (01)60889971019394(21)2251
    • (01)60889971019394(21)2252
    • (01)60889971019394(21)2253
    • (01)60889971019394(21)2259
    • (01)60889971019394(21)2264
    • (01)60889971019394(21)2265
    • (01)60889971019394(21)2266
    • (01)60889971019394(21)2267
    • (01)60889971019394(21)2270
    • (01)60889971019394(21)2271
    • (01)60889971019394(21)2272
    • (01)60889971019394(21)2273
    • (01)60889971019394(21)2274
    • (01)60889971019394(21)2275
    • (01)60889971019394(21)2276
    • (01)60889971019394(21)2277
    • (01)60889971019394(21)2278
    • (01)60889971019394(21)2279
Amount recalled
3,961 units

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Unexpected failure of electrical components within the CPI generator.

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, 5:42 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.