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Unnamed device
Model 5450040001 · STRYKER CORPORATION · DI 07613252468271
ERL — Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece · Class II · 21 CFR 874.4250
UDILibrary device dossier · generated 2026-09-06 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.
Recall history (0)
No recalls linked in the loaded window.
Adverse-event reports — MAUDE (409)
Caveat (required reading): 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 is a reporting baseline (average device in the same product code), not a risk measure.
Malfunction: 409
Monthly adverse-event reports for this device versus the product-code average.
Month
This device (reports)
Product-code average (reports per device)
2019-01
4
4.2
2019-02
6
3.58
2019-03
3
6.27
2019-04
6
5.47
2019-05
3
3.92
2019-06
2
4.13
2019-07
2
4.17
2019-08
7
5.32
2019-09
5
4.17
2019-10
6
4.24
2019-11
5
5.24
2019-12
6
5.06
2020-01
1
4.4
2020-02
3
3.92
2020-03
13
4.79
2020-04
1
4.51
2020-05
2
2.98
2020-06
1
5.68
2020-07
7
5.4
2020-08
7
4.57
2020-09
8
4.43
2020-10
5
5.14
2020-11
6
4.88
2020-12
7
5.08
2021-01
2
4.86
2021-02
2
5.1
2021-03
10
5.73
2021-04
3
4.56
2021-05
5
4.56
2021-06
4
5.43
2021-07
3
4.49
2021-08
5
4.87
2021-09
4
3.93
2021-10
2
3.19
2021-11
10
4.08
2021-12
5
3.67
2022-01
11
3.52
2022-02
3
3.15
2022-03
9
3.37
2022-04
3
3.75
2022-05
7
2.97
2022-06
8
4.16
2022-07
6
4.17
2022-08
4
4.26
2022-09
2
3.72
2022-10
9
4.13
2022-11
4
4.3
2022-12
5
4.24
2023-01
9
3.42
2023-02
4
3.95
2023-03
2
4.6
2023-04
2
4
2023-05
0
5.03
2023-06
5
3.99
2023-07
2
4.33
2023-08
8
3.73
2023-09
8
3.85
2023-10
7
3.6
2023-11
1
3.86
2023-12
3
3.34
2024-01
2
4.05
2024-02
2
4.64
2024-03
16
4.32
2024-04
19
4.26
2024-05
2
3.3
2024-06
2
3.43
2024-07
0
3.6
2024-08
3
3.6
2024-09
1
4.95
2024-10
6
4.01
2024-11
1
3.64
2024-12
2
3.46
2025-01
2
2.95
2025-02
1
6.82
2025-03
7
4.95
2025-04
0
3.08
2025-05
3
4.42
2025-06
2
3.56
2025-07
8
3.98
2025-08
4
3.5
2025-09
4
3.1
2025-10
0
3.8
2025-11
2
3.27
2025-12
8
3.46
2026-01
4
2.62
2026-02
2
3.38
2026-03
1
3.6
2026-04
2
5.25
2026-05
10
3.94
2026-06
0
4.1
This device (reports/month)Average device in ERL (reports/device/month)
Regulatory clearances
None linked in the loaded window.
Manufacturer compliance record — STRYKER CORPORATION
Warning Letter 2017-04-06 Entellus Medical Inc.
Warning Letter 2015-04-08 Thermedx LLC
Injunction 2013-11-26 Physio-Control, Inc.
Warning Letter 2013-03-06 Stryker Corporation
Warning Letter 2013-03-06 Stryker Corporation
NAI 2026-06-18 International Life Sciences · 0 citations
VAI 2026-02-20 Stryker Puerto Rico, LLC · 2 citations
NAI 2025-12-11 Stryker Manufacturing Kalamazoo · 0 citations
NAI 2025-05-22 Stryker Macroom · 0 citations
VAI 2025-03-27 Stryker GmbH · 1 citations
VAI 2025-03-27 Stryker GmbH · 1 citations
NAI 2025-02-27 Stryker Leibinger GmbH & Co. KG · 0 citations
NAI 2025-01-30 Serf · 0 citations
VAI 2024-12-18 Stryker Neurovascular · 1 citations
VAI 2024-11-15 Stryker Medical Division of Stryker Corporation · 2 citations
NAI 2024-11-13 POM Medical LLC · 0 citations
VAI 2024-07-25 Stryker Ireland, Ltd., Instruments Division · 1 citations
NAI 2024-05-03 Stryker Neurovascular, Inc. · 0 citations
NAI 2024-04-18 Physio-Control, Inc. · 0 citations
VAI 2023-12-01 Howmedica Osteonics Corp. · 1 citations
VAI 2023-05-15 LimFlow, Inc. · 2 citations
NAI 2023-04-25 Stryker Puerto Rico, LLC · 0 citations