Stryker Corporation
126 federal recalls on file, showing the 38 from the last 12 months. We monitor every CPSC, FDA, USDA, and NHTSA notice for Stryker Corporation and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-03-25FDA-DeviceClass IICheck your Stryker Cub crib serial number
Some Stryker Cub Pediatric Cribs sold in the USA are missing two warning labels on the access doors. This affects 590 cribs with specific serial numbers. No injuries have been reported.
- 2026-02-25FDA-DeviceClass IICheck your Stryker MOLLI 2 system serial number
Stryker is recalling certain MOLLI 2 surgical marker systems because the instructions for use need to be updated. Magnetized surgical tools used during the procedure may dislodge the markers that are placed to mark the surgical site. Stryker is providing updated labeling to address this issue.
- 2025-12-17FDA-DeviceClass IIDo not use Stryker Arise mattress with MV3 bed
Stryker recalled certain Arise 1000EX mattresses because some were sold near MV3 beds, raising concern they might be used together. The mattress and bed have not been tested together and are not designed to work as a pair. Using them together is not recommended by Stryker.
- 2025-12-17FDA-DeviceClass IICheck your Stryker MV3 bed serial number
Stryker recalled certain MV3 bariatric beds because some were sold near Arise 1000EX mattresses, suggesting they might be used together. The bed and mattress have not been tested for compatibility and should not be used together.
- 2025-12-03FDA-DeviceClass IINICO BrainPath; Product Number/Product Name NN-8024 BrainPath Shephard's Hook - Greenberg; NN-8025 BrainPath Shephard's Hook - Sugita; NN-8026 BrainPath Shephard's Hook - Budde; NN-8042 BrainPath Shephard's Hook - Greenberg LK;
Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.
- 2025-12-03FDA-DeviceClass IINICO Myriad Illumination Pack Product No. NN-1000 11g Illumination Sleeve/Fiber; Product No. NN-1001 13g Illumination Sleeve/Fiber
Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.
- 2025-12-03FDA-DeviceClass IINICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP; NN-8001 15x 13 MHP; NN-8002 15x 25 MHP - MINOP; NN-8003 13x10 MHP; NN-8004 13x13 MHP; NN-8005 15x25 MHP GAAB; NN-8006 11X10 MHP; NN-8007 11x13 MHP; NN-8008 19x28 MHP OI; NN-8010 17x31.5 MHP DECQ; NN-8015 NICO Fluid System (NFS); NN-8017 11x13 MHP/PB; NN-8018 13X13 MHP/PB; NN-8019 19x28 MHP Little LOTTA; NN-8020 19x21.5 MHP PaediScope; NN-8021 15x26.5 MHP LOTTA; NN-8500 15x10 MHP; NN
Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.
- 2025-11-19FDA-DeviceClass IIHARMONIC FOCUS Shears + Adaptive Tissue Technology, 9 cm Length REF: HAR9F, Reprocessed Device for Single Use, STERILEEO, RX ONLY
Due to manufacturing issue, reprocessed shears, may become stuck in the "on position" resulting in continuous activation.
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