Reported Oct 8, 2014 · Terminated

CelluTome Epidermal Harvesting System Part number CT-H25 or Part Number CT-H50

KCI USA, 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: KCI USA, Inc. · 6203 Farinon Dr · San Antonio, TX · 78249-3441

Is this the product you have?

  • CelluTome Epidermal Harvesting System Part number CT-H25 or Part Number CT-H50
Lot codes and dates
  • Part number
  • CT-H25 with the following lot numbers
    • 3244680000
    • 3446210000
    • 3246280000
    • 3246480000
    • 3246490000
    • 3246970000
    • 3247020000
    • 3247030000
    • 3247130000
    • 3247440000
    • 3247670000
    • 3247680000
    • 3247980000
    • 3248070000
    • 3248200000
    • 3248300000
    • 3249120000
    • 3249130000
    • 3249140000
    • 3249150000
    • 3249160000. Part number
  • CT-H50 with the following lot numbers
    • 324782
    • 324796
    • 324797
    • 3245120000
    • 3245670000
    • 3245680000
    • 3246270000
    • 3246490000
    • 3246690000
    • 3246700000
    • 3246940000
    • 3246980000
    • 3247140000
    • 3247160000
    • 3247170000
    • 3247250000
    • 3247310000
    • 3247470000
    • 324780000
    • 3247810000
    • 3247820000
    • 3247960000
    • 3247970000
    • 3248080000
    • 3248190000
    • 3248230000
    • 3248300000
    • 3248380000
    • 3248960000
    • 3248970000
    • 3248980000
    • 3248990000
    • 3249000000
    • 3249010000
    • 3249020000
    • 3249030000
    • 3249040000
    • 3249050000
    • 3249060000
    • 3249070000
    • 3249080000
    • 3249090000
    • 3249100000
    • 3249110000
    • 3249390000
    • 3249580000
Amount recalled
1,331 units

Where it was sold

  • Nationwide

Why it was recalled

Blade can shift during shipping which makes the product ineffective.

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

Notice updated Sep 18, 2015 · Data as of Sep 19, 6:16 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.