Stryker Sustainability Solutions Lakeland
FDA adverse event reports naming Stryker Sustainability Solutions Lakeland as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER SUSTAINABILITY SOLUTIONS LAKELAND.
- Total reports
- 1,154
- Deaths
- 4
- Injuries
- 212
- Malfunctions
- 938
Reports per year
20213
14514
13215
17616
15617
7818
6319
9020
6621
4222
323
124
Source: FDA adverse event reports by year received, 2013–2024. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Single-Use Reprocessed Ultrasonic Surgical InstrumentsNLQ446
- Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, ReprocessedNUJ309
- ArthroscopeHRX207
- Tourniquet, PneumaticKCY79
- Laparoscope, General & Plastic Surgery, ReprocessedNLM42
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI34
- Hysteroscope (And Accessories)HIH7
- Oximeter, ReprocessedNLF7
- OximeterDQA6
- Instrument, Ultrasonic SurgicalLFL5
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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