Reported Jun 15, 2022 · Ongoing

STORZ KARL STORZ-ENDOSKOPE REF 11272VUE CMOS Video Cysto-Urethroscope REF 11272VUEK CMOS Video Cysto-Urethroscope…

Karl Storz Endoscopy

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: Karl Storz Endoscopy · 2151 E Grand Ave · El Segundo, CA · 90245-5017

Is this the product you have?

4 of 4 products

Products covered by this recall
Model / numberProduct as published
11272VUECMOS Video Cysto-Urethroscope
11272VUEKCMOS Video Cysto-Urethroscope C-VIEW KIT
11272VUE-RCMOS Video Cysto-Urethroscope
11272VUEK-RCMOS Video Cysto-Urethroscope C-VIEW KIT
Lot codes and dates
  • Scope Base Part Number(s)11272VUE
  • Scope Kit Part Number11272VUEK
  • UDI Code-DI4048551431382
  • Serial Numbers

    337 of 337 codes

    • 25407
    • 32321
    • 38539
    • 53439
    • 58011
    • 58143
    • 58546
    • 59051
    • 25408
    • 32389
    • 40370
    • 53574
    • 58020
    • 58144
    • 58557
    • 59063
    • 25410
    • 32391
    • 40371
    • 53575
    • 58021
    • 58145
    • 58558
    • 59093
    • 25766
    • 32417
    • 40707
    • 53589
    • 58022
    • 58156
    • 58567
    • 59094
    • 28096
    • 32994
    • 40708
    • 53593
    • 58045
    • 58157
    • 58569
    • 59095
    • 28257
    • 33787
    • 41249
    • 53627
    • 58046
    • 58183
    • 58570
    • 59096
    • 28919
    • 33802
    • 44912
    • 53628
    • 58047
    • 58184
    • 58663
    • 59098
    • 29286
    • 33804
    • 45546
    • 53632
  • Scope Kit Number(s)11272VUK-R
  • Scope Kit Part Number11272VUEK-R
  • UDI Code-DI4048551444351
  • Serial Numbers

    64 of 64 codes

    • 25894
    • 37977
    • 48678
    • 58399
    • 59872
    • 60163
    • 60316
    • 60930
    • 25898
    • 38237
    • 49374
    • 58424
    • 59873
    • 60164
    • 60325
    • 61141
    • 27983
    • 38542
    • 49376
    • 58467
    • 59874
    • 60208
    • 60388
    • 61142
    • 30293
    • 40571
    • 51596
    • 58468
    • 59875
    • 60209
    • 60420
    • 61232
    • 31667
    • 40572
    • 55498
    • 58512
    • 59876
    • 60298
    • 60429
    • 61234
    • 31730
    • 40706
    • 57611
    • 58645
    • 60022
    • 60302
    • 60512
    • 61268
    • 32409
    • 44105
    • 58122
    • 58711
    • 60023
    • 60303
    • 60724
    • 61269
    • 34423
    • 46522
    • 58398
    • 59554
Amount recalled
401 units

Where it was sold

Why it was recalled

The endoscope may experience a loss of image when activating monopolar electrocautery, due a manufacturing assembly process issue.

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, 7:41 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.