Every recall we track for Stryker Instruments Div. of Stryker Corporation — 38 in all — plus the complaints and injury reports the public filed about them.
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.
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.
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.
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.
Stryker recalls telescopic smoke evac pencils with hairline fractures that could cause electrical arcing and burns. Affected models include Product No. SHKTSPCL, sold with UDI GTIN 37613327466332.
Stryker recalls telescopic Bovie pencils with product number SHK TSPL due to potential hairline fractures causing electrical arcing and burns. Affected units may have a 75-inch length and specific UDI codes.
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.
Stryker recalls disposable tourniquet cuffs that may leak air, causing blood flow loss during surgery. Affected units have specific product numbers and lot numbers. Consumers should contact Stryker for details.
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.
Stryker recalls C2 Nerve Monitor models due to possible use errors causing nerve injury during surgery. Affected units include specific serial numbers and models.
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.
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.
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.
Stryker recalls specific lot numbers of T5 Zipper Toga with Peel-Away Face Shield for potential contaminant exposure due to material layer separation. Affected units include catalog 0400-820-100 with listed lot numbers.
Stryker recalls sterile T4 Pullover Toga Large garments with specific lot numbers due to potential separation of material layers that could expose users to contaminants.
Stryker recalls sterile T4 Pullover Toga garments due to potential material layer separation causing contaminant exposure. Affected items have lot number 17061792.
Stryker recalls sterile T4 Pullover Toga (S/M) due to potential material layer separation causing contaminant exposure. Affected units have catalog number 0400-710-000.
Stryker recalls X-Large T4 Pullover Toga sterile garments due to potential material layer separation causing contaminant exposure. Affected units have specific lot numbers.
Stryker recalls sterile surgical gowns with lot numbers 17061810-17113221 due to potential material layer separation causing contaminant exposure. Affected users should contact Stryker for replacement.
Stryker recalls sterile protective garments with lot numbers 17113139 and 17113204 due to potential material layer separation causing contaminant exposure.
Stryker recalls sterile surgical toga garments with lot numbers 17113078, 17113132, 17113138 due to potential material layer separation causing contaminant exposure.
Stryker recalls sterile surgical gowns with peel-away face shields due to potential contaminant exposure from material layer separation. Affected items have specific catalog and lot numbers.
Stryker recalls X-Large T4 Zipper Toga sterile garments with lot numbers 17061835-17113223 due to potential material layer separation causing contaminant exposure. Affected users should contact Stryker for details.
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.
Stryker recalls 180-gram cement cartridges with higher bioburden levels than safe limits for orthopedic surgery. Affected units may cause infections if used without proper sterilization.
Stryker recalls InterPulse handpieces with higher-than-expected bioburden levels that may compromise sterility during orthopedic surgery.
Stryker recalls Revolution 90 Degree Tibial Nozzle (Product Number 0606-516-000) due to higher bioburden levels than acceptable, risking infection during orthopedic surgery.
Stryker recalls AutoPlex System bone cement products due to higher bioburden levels than acceptable, potentially causing contamination. Affected units include specific product numbers and lot numbers.
Stryker recalls Break-Away Femoral Nozzle (Product #0206-512-000) due to higher bioburden levels risking infection during orthopedic surgery. Affected units sold with Lot Number 17279012.
Stryker recalls two models of femoral canal pressurizers due to higher than expected bioburden levels, potentially causing contamination. Affected units have specific product numbers and lot numbers.
Stryker recalls orthopedic cement kits with higher bioburden levels than safe limits. Affected kits may cause infections if used without proper sterility.
Stryker recalls two spinal orthopedic iVAS System Kits due to higher bioburden levels than acceptable, risking infection during surgery. Affected kits have specific product numbers and lot dates.
Stryker recalls 10g/15mm iVAS System Kit (Product #0705-115-000) due to higher bioburden levels risking infection during spinal surgery. Affected units sold with Lot #17283012.
Stryker recalls 11g Verteport Cement Cannulas (18/pkg) for spinal surgery due to higher bioburden levels risking infection. Affected units have Product Number 0306-511-000 and UDI (01)7613252594307.
Stryker recalls specific spinal orthopedic kits due to higher bioburden levels than acceptable, risking infection. Affected kits have product number 0506-485-000 and UDI (01)4546540907035.
Stryker recalls certain orthopedic Intramedullary Brushes due to higher bioburden levels than acceptable, risking contamination during surgery. Affected units have specific product numbers and lot numbers.
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.
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.
