Stryker Instruments Div. of Stryker Corporation recalls
Every recall we track for Stryker Instruments Div. of Stryker Corporation — 38 in all, from 2017–2022 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Stryker Instruments Div. of Stryker Corporation peaked in 2017 (14); 38 since 2017.
All FDA recall records for Stryker Instruments Div. of Stryker Corporation since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 1 | 12 | 1 | 14 |
| 2018 | 0 | 0 | 12 | 0 | 12 |
| 2019 | 0 | 1 | 4 | 0 | 5 |
| 2020 | 0 | 4 | 2 | 0 | 6 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 1 | 0 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Stryker Instruments Div. of Stryker Corporation product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Stryker Instruments Div. of Stryker Corporation recalls
12 shown- Use cautionMedical device
Stryker Instruments Div. of Stryker Corporation recalls SurgiCount+ System Application, Software Version 2.0.17, Catalog Number 0694-002-090. Used for counting, displaying,
Stryker recalls SurgiCount+ software version 2.0.17 due to potential duplicate sponge counting errors during surgery. This could lead to retained surgical sponges if not corrected. Update to prevent the error.
StrykerJun 15, 2022 - Use cautionMedical device
Stryker Instruments Div. of Stryker Corporation recalls Stryker Zyphr Disposable Cranial Perforator, Large 14/11 mm- is a sterile, single use cutting accessory intended for
Stryker recalls large 14/11 mm disposable cranial perforators due to potential cracks that could cause metal fragments in surgical sites or delayed disengagement. Affected units have specific lot numbers.
StrykerOct 16, 2020 - Lower riskMedical device
Stryker Instruments Div. of Stryker Corporation recalls Neptune E-SEP 165mm Blade Electrode, Catalog Number 0703-165-001 - Product Usage: The Neptune E-SEP is an Integrated
Stryker recalls Neptune E-SEP 165mm Blade Electrode (Lot 16240231) due to expired product from a distribution error. This may not affect safety but requires checking the lot number.
StrykerMar 26, 2020 - Lower riskMedical device
Stryker Instruments Div. of Stryker Corporation recalls Triton Canister System (finished part numbers FG 12009, for 3L canisters, and FG 12019 for 2L canisters) Scanning Label
Stryker recalls Triton Canister Scanning Labels made before Dec 2019 due to potential underestimation of blood loss during surgery. Affected labels have specific part numbers and manufacturing dates.
StrykerJan 22, 2020 - Use cautionMedical device
Stryker Instruments Div. of Stryker Corporation recalls SafeAir Telescopic Smoke Evacuation Pencil, Product No. 0703 046 004. The product is a Bovie pencil that is 75 inches
Stryker recalls a 75-inch telescopic smoke evacuation pencil due to potential hairline fractures causing electrical arcing and burns to users or patients. Affected units have specific product numbers.
StrykerJan 13, 2020 - Use cautionMedical device
Stryker Instruments Div. of Stryker Corporation recalls Color Cuff Disposable Tourniquet Cuff, 18 inch X 3 inch, 1BLA (Single Bladder), 2PRT(Dual Port) Quick Connect
Stryker recalls disposable tourniquet cuffs that may leak air, causing loss of blood flow during surgery. Affected units have specific model and lot numbers. Consumers should contact Stryker for details.
StrykerNov 6, 2019 - Lower riskMedical device
Stryker Instruments Div. of Stryker Corporation recalls C2 Nerve Monitor, 8 Channel, 5140-508-280, UDI 07613327277319 Product Usage: The C2 Nerve Monitor System is intended
Stryker recalls C2 Nerve Monitor models due to possible use errors causing nerve injury during surgery. Affected units include specific serial numbers and models sold for intra-operative nerve monitoring.
StrykerJul 31, 2019 - Lower riskMedical device
Stryker Instruments Div. of Stryker Corporation recalls Performance Series Sagittal Blade, Catalog Number 6125-127-100 Product Usage: The Stryker Heavy Duty Sagittal Blades
Stryker recalls heavy duty sagittal blades (catalog 6125-127-100) due to potential sterility breach during manufacturing. Affected units may not be sterile, risking infection during surgery.
StrykerMar 19, 2019 - Lower riskMedical device
Stryker Instruments Div. of Stryker Corporation recalls Triton Sponge System (Software), GAUS-3, Software Versions 4.6.5, 4.8.7, 4.9.6
Stryker recalls Triton Sponge System software versions 4.6.5, 4.8.7, and 4.9.6 for updated instructions on sponge handling and calibration placards.
StrykerDec 4, 2018 - Lower riskMedical device
Stryker Instruments Div. of Stryker Corporation recalls T4 Zipper Toga (S/M); Catalog Number: 0400-810-000 Sterile personal protection garment
Stryker recalls sterile T4 Zipper Toga (S/M) garments with catalog number 0400-810-000 due to potential material layer separation causing contaminant exposure. Affected items may be at risk of exposure to harmful substances.
StrykerFeb 23, 2018 - Lower riskMedical device
Stryker Instruments Div. of Stryker Corporation recalls Revolution CMS w/ Femoral Breakaway Nozzle & Med. Press., Product Number: 0606-573-000, UDI: (01)4546540912114 for
Stryker recalls Revolution CMS surgical devices with higher-than-acceptable bioburden levels. These devices may not be sterile, risking infections during orthopedic procedures. Affected units have specific product numbers and lot numbers.
StrykerNov 9, 2017 - Use cautionMedical device
Stryker Instruments Div. of Stryker Corporation recalls The Stryker Thoracic Pedicle Feeler 6002-350-000 is a smart instrument for remote control of the navigation software
Stryker recalls specific Thoracic Pedicle Feelers (serials 10897-10928) due to potential tip breakage from material degradation. Learn what to do if you own this instrument.
StrykerOct 16, 2017
Stryker Instruments Div. of Stryker Corporation recall questions
How many recalls has Stryker Instruments Div. of Stryker Corporation had?
38 recalls from Stryker Instruments Div. of Stryker Corporation are on record with U.S. safety agencies, from 2017–2022.
What is the most recent Stryker Instruments Div. of Stryker Corporation recall?
Stryker Instruments Div. of Stryker Corporation recalls SurgiCount+ System Application, Software Version 2.0.17, Catalog Number 0694-002-090. Used for counting, displaying,, dated Jun 15, 2022. Every Stryker Instruments Div. of Stryker Corporation recall is listed on this page, newest first.
What should I do if I have a recalled Stryker Instruments Div. of Stryker Corporation product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Stryker Instruments Div. of Stryker Corporation recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.