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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 reportMalfunction 1
61218242019-08: 0 reports for this device; peer average 2/device2020-04: 0 reports for this device; peer average 2/device2020-09: 0 reports for this device; peer average 1/device2020-12: 0 reports for this device; peer average 2/device2021-05: 0 reports for this device; peer average 2/device2021-07: 0 reports for this device; peer average 3/device2021-09: 0 reports for this device; peer average 1/device2021-11: 0 reports for this device; peer average 3/device2021-12: 0 reports for this device; peer average 1/device2022-02: 0 reports for this device; peer average 1/device2022-07: 0 reports for this device; peer average 1/device2023-01: 0 reports for this device; peer average 2/device2023-02: 0 reports for this device; peer average 23.5/device2023-03: 0 reports for this device; peer average 15/device2023-04: 0 reports for this device; peer average 6/device2023-05: 0 reports for this device; peer average 2/device2023-06: 0 reports for this device; peer average 1/device2023-07: 0 reports for this device; peer average 1/device2023-08: 0 reports for this device; peer average 1/device2023-10: 0 reports for this device; peer average 9/device2024-01: 0 reports for this device; peer average 8.67/device2024-02: 0 reports for this device; peer average 1/device2024-03: 0 reports for this device; peer average 9/device2024-04: 0 reports for this device; peer average 3.5/device2024-05: 0 reports for this device; peer average 1/device2024-06: 0 reports for this device; peer average 2/device2024-09: 0 reports for this device; peer average 1/device2024-10: 0 reports for this device; peer average 1/device2025-01: 0 reports for this device; peer average 3/device2025-02: 0 reports for this device; peer average 2.67/device2025-03: 0 reports for this device; peer average 1/device2025-04: 1 reports for this device; peer average 1.5/device2025-05: 0 reports for this device; peer average 1.5/device2025-08: 0 reports for this device; peer average 1.33/device2025-10: 0 reports for this device; peer average 1.5/device2025-11: 0 reports for this device; peer average 1/device2025-12: 0 reports for this device; peer average 6/device2026-01: 0 reports for this device; peer average 6/device2026-02: 0 reports for this device; peer average 1.5/device2026-03: 0 reports for this device; peer average 4.4/device2026-04: 0 reports for this device; peer average 5.33/device2026-05: 0 reports for this device; peer average 2.2/device2026-06: 0 reports for this device; peer average 4/device08040912050709111202070102030405060708100102030405060910010203040508101112010203040506
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0802
2020-0402
2020-0901
2020-1202
2021-0502
2021-0703
2021-0901
2021-1103
2021-1201
2022-0201
2022-0701
2023-0102
2023-02023.5
2023-03015
2023-0406
2023-0502
2023-0601
2023-0701
2023-0801
2023-1009
2024-0108.67
2024-0201
2024-0309
2024-0403.5
2024-0501
2024-0602
2024-0901
2024-1001
2025-0103
2025-0202.67
2025-0301
2025-0411.5
2025-0501.5
2025-0801.33
2025-1001.5
2025-1101
2025-1206
2026-0106
2026-0201.5
2026-0304.4
2026-0405.33
2026-0502.2
2026-0604
This device (reports/month)Average device in FTA (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
2025-04-2321890122MalfunctionAvailablemodel number
Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2017-11-08VAIVoluntary action indicatedAspen Surgical Products, Inc.5
2017-11-08VAIVoluntary action indicatedAspen Surgical Products, Inc.5
2017-03-02NAINo action indicatedAspen Surgical Products Inc0
2015-11-03NAINo action indicatedAspen Surgical Puerto Rico Corp.0
2015-02-11NAINo action indicatedAspen Surgical Products, Inc.0
2015-02-11NAINo action indicatedAspen Surgical Products, Inc.0
2014-07-01NAINo action indicatedAspen Surgical Products Inc0
2013-02-15VAIVoluntary action indicatedAspen Surgical Products, Inc.1
2013-02-15VAIVoluntary action indicatedAspen Surgical Products, Inc.1
2012-09-28NAINo action indicatedAspen Surgical Products Inc0
2010-02-26VAIVoluntary action indicatedAspen Surgical Products, Inc.4
2010-02-26VAIVoluntary action indicatedAspen Surgical Products, Inc.4
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