Olympus A22052ARecalls & reported problems
OLYMPUS Winter & Ibe GmbH · Irrigation port, 1 Luer-Lock connector, rotatable · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04042761021036), received between Jun 24, 2021 and Jun 24, 2021 — classified as 1 injury.
18 other recalls cover devices cleared under the same FDA submission (K931994, K931995); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Burn(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 24, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
UPDATE: THE CUSTOMER CLARIFIED 02JUL2021 THAT THE CUSTOMER DOES NOT USE AN OLYMPUS GENERATOR OR OLYMPUS GROUNDING PADS. THE BURN EXPERIENCED BY THE PATIENT IS NOT RELATED TO THE USE OF AN OLYMPUS DEVICE.
Patient problems: Burn(s)
MAUDE report 12063820 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K931994, K931995. One submission often covers many models, so check the product and lot details in each record.
- Z-1455-2026 · Nov 11, 2025 · Open, ClassifiedOlympus Inner Sheath. Model No. A2641. for endoscopic diagnosis and treatment in urological applications.
- Z-1440-2026 · Nov 11, 2025 · Open, ClassifiedOlympus Resection Inner Sheath for 26 Fr. Outer Sheath. Model No. A22040T. Resection sheath for urologic applications.
- Z-1448-2026 · Nov 11, 2025 · Open, ClassifiedOlympus Resection Sheath, 8 mm. Model No. A42011A. Resection sheath for gynecological applications.
- Z-1444-2026 · Nov 11, 2025 · Open, ClassifiedOlympus Resection Sheath, 26 Fr. with Deflecting Obturator; Model No. A22042T. Resection sheath for urologic applications.
- Z-1451-2026 · Nov 11, 2025 · Open, ClassifiedOlympus Inner Sheath, Long; Model No. WA22017T. Inner sheath for urological and gynecological applications.
- Z-1452-2026 · Nov 11, 2025 · Open, ClassifiedOlympus Resection Sheath; Model No. A2666. Resection sheath for urologic applications.
- Z-1443-2026 · Nov 11, 2025 · Open, ClassifiedOlympus Resection Sheath, 26 Fr.; Model No. A22042A. Resection sheath for urologic applications.
- Z-1447-2026 · Nov 11, 2025 · Open, ClassifiedOlympus Inner Sheath; Model No. A2660. for endoscopic diagnosis and treatment in urological applications.
- Z-1453-2026 · Nov 11, 2025 · Open, ClassifiedOlympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic diagnosis and treatment in urological applications.
- Z-1457-2026 · Nov 11, 2025 · Open, ClassifiedOlympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and treatment in urological applications.
- Z-1450-2026 · Nov 11, 2025 · Open, ClassifiedOlympus Inner Sheath, Long; Model No. WA22017A. Inner sheath for urological and gynecological applications.
- Z-1456-2026 · Nov 11, 2025 · Open, ClassifiedOlympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and treatment in urological applications.
- Z-1441-2026 · Nov 11, 2025 · Open, ClassifiedOlympus Resection Sheath, 24 Fr; Model No. A22041A. Resection sheath for urologic applications.
- Z-1439-2026 · Nov 11, 2025 · Open, ClassifiedOlympus Resection Inner Sheath, for 26 Fr. Outer Sheath. Model No. A22040A. Resection sheath for urologic applications.
- Z-1445-2026 · Nov 11, 2025 · Open, ClassifiedOlympus Resection Sheath, 28 Fr.; Model No. A22043A. Resection sheath for urologic applications.
…and 3 more.
Other Resectoscope devices
- Olympus A22040AOLYMPUS Winter & Ibe GmbH · Resectoscope1 recall1,764 reports
- Olympus A42011AOLYMPUS Winter & Ibe GmbH · Resectoscope1 recall963 reports
- Olympus A22041AOLYMPUS Winter & Ibe GmbH · Resectoscope1 recall656 reports
- Olympus A22042AOLYMPUS Winter & Ibe GmbH · Resectoscope1 recall55 reports
- Olmypus WA22017AOLYMPUS Winter & Ibe GmbH · Resectoscope1 recall31 reports
- Olympus A22040TOLYMPUS Winter & Ibe GmbH · Resectoscope1 recall23 reports
- Olympus A22041TOLYMPUS Winter & Ibe GmbH · Resectoscope1 recall12 reports
- Olympus A22014AOLYMPUS Winter & Ibe GmbH · Resectoscope1 recall11 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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