Data Foundry

Medical device recalls 2022

STORZ KARL STORZ-ENDOSKOPE REF 11272VUE CMOS Video Cysto-Urethroscope… — Class II medical device recall Z-1234-2022

Ongoing recall by Karl Storz Endoscopy, reported 2022-06-15, distributed nationwide. The endoscope may experience a loss of image when activating monopolar electrocautery, due a manufacturing ass

Recall numberZ-1234-2022
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmKarl Storz Endoscopy, El Segundo, CA, United States
Recall initiated2022-05-03
Classified2022-06-03
Reported by FDA2022-06-15
DistributedNationwide (US)
Countries outside the USCA
Quantity401 units
UPC / GTIN / UDI-DI04048551431382, 04048551444351
Serial numbers25407, 25408, 25410, 25766, 25894, 25898, 27983, 28096, 28257, 28919, 29286, 29342, 30054, 30293, 30881, 31033, 31036, 31038, 31300, 31302, 31374, 31413, 31533, 31622, 31667 and 376 more
Model numbers11272VUE, 11272VUE-R, 11272VUEK, 11272VUEK-R

Product

STORZ KARL STORZ-ENDOSKOPE REF 11272VUE CMOS Video Cysto-Urethroscope REF 11272VUEK CMOS Video Cysto-Urethroscope C-VIEW KIT REF 11272VUE-R CMOS Video Cysto-Urethroscope REF 11272VUEK-R CMOS Video Cysto-Urethroscope C-VIEW KIT

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1234-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.