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Adverse-event reports (MAUDE)

Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.

1 linked reportInjury 1
12342020-11: 0 reports for this device; peer average 1/device2021-03: 0 reports for this device; peer average 4/device2021-05: 0 reports for this device; peer average 1/device2021-06: 0 reports for this device; peer average 1/device2021-07: 0 reports for this device; peer average 1/device2021-08: 0 reports for this device; peer average 2/device2021-09: 0 reports for this device; peer average 1/device2021-12: 0 reports for this device; peer average 1/device2022-04: 0 reports for this device; peer average 1/device2022-06: 0 reports for this device; peer average 1/device2022-08: 0 reports for this device; peer average 2/device2023-04: 0 reports for this device; peer average 1/device2023-06: 0 reports for this device; peer average 2/device2023-07: 0 reports for this device; peer average 1/device2023-08: 0 reports for this device; peer average 1/device2023-12: 0 reports for this device; peer average 1.33/device2024-01: 0 reports for this device; peer average 1/device2024-02: 0 reports for this device; peer average 1/device2024-03: 0 reports for this device; peer average 2/device2024-06: 0 reports for this device; peer average 1/device2024-08: 0 reports for this device; peer average 1/device2024-12: 0 reports for this device; peer average 2/device2025-01: 0 reports for this device; peer average 2/device2025-03: 0 reports for this device; peer average 3/device2025-04: 0 reports for this device; peer average 1.5/device2025-05: 1 reports for this device; peer average 1/device2025-07: 0 reports for this device; peer average 1/device2025-10: 0 reports for this device; peer average 1/device2025-11: 0 reports for this device; peer average 1/device2025-12: 0 reports for this device; peer average 3/device2026-03: 0 reports for this device; peer average 1/device2026-04: 0 reports for this device; peer average 1/device1103050607080912040608040607081201020306081201030405071011120304
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2020-1101
2021-0304
2021-0501
2021-0601
2021-0701
2021-0802
2021-0901
2021-1201
2022-0401
2022-0601
2022-0802
2023-0401
2023-0602
2023-0701
2023-0801
2023-1201.33
2024-0101
2024-0201
2024-0302
2024-0601
2024-0801
2024-1202
2025-0102
2025-0303
2025-0401.5
2025-0511
2025-0701
2025-1001
2025-1101
2025-1203
2026-0301
2026-0401
This device (reports/month)Average device in HRM (reports/device/month)
Failure-mode summaryAI-generated

1 linked report narrative available — no AI summary generated yet.

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2025-05-309615010-2025-00010InjuryAvailableexact di
Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2024-03-26NAINo action indicatedCarl Zeiss Meditec Inc.0
2018-10-25NAINo action indicatedCarl Zeiss Meditec Inc.0
2017-02-24NAINo action indicatedCarl Zeiss Meditec AG0
2016-03-25NAINo action indicatedCarl Zeiss Meditec Inc.0
2014-09-18NAINo action indicatedCarl Zeiss Meditec Inc.0
2014-08-15NAINo action indicatedCarl Zeiss Meditec AG0
2014-03-26NAINo action indicatedCarl Zeiss Meditec Inc.0
2011-11-17NAINo action indicatedCarl Zeiss Meditec Inc.0
2011-06-22NAINo action indicatedCarl Zeiss Meditec Inc.0
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