Stryker Corporation recalls

Stryker Leibinger is recalling Precision Pointer Electromagnetic devices because the pointer tube can crack at a laser-welded joint during use. If that happens, loose parts could fall out while the device is inside a patient. No injuries have been reported.

Moderate·FDA·Oct 29, 2026

Stryker Sustainability Solutions is recalling a specific lot of BARD EP XT Decapolar Steerable diagnostic catheters (Reference 201007) used in heart rhythm procedures. Some units may have a compromised sterile barrier on the primary pouch packaging, which could allow contamination if the catheter is used. This poses a risk of particle buildup, infection, or blood clots.

Moderate·FDA·Oct 14, 2026

Stryker is recalling six Ethicon XCEL bladeless trocar products, which are reusable surgical access port systems. The ports may crack or separate during use. No injuries have been reported.

Moderate·FDA·Sep 23, 20266 products

Stryker Neurovascular's INZONE Detachment System devices may experience premature battery drain, causing them to fail to power on, display faint indicators, or be unable to detach an embolization coil as intended. If a device fails during a procedure, medical staff may need to use an alternative technique to complete the intervention.

Moderate·FDA·Jul 1, 2026

Stryker is recalling 26 reprocessed electrophysiology catheters because their sterile packaging seals may be incomplete. The products were distributed across the US and to Israel and Canada. No injuries have been reported.

Moderate·FDA·May 20, 202626 products

Stryker Corporation recalled a limited lot of FluidSmart Urology Tube Sets (REF LL0006) used with fluid management systems in surgical procedures. Some units in this lot did not meet manufacturing standards. No injuries have been reported.

Moderate·FDA·May 20, 2026

Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.

FDA·Apr 15, 2026

The surgical light assembly in Stryker CHROMOPHARE Softlit Ring systems may not adequately support the weight of the ceiling cover. This could potentially cause the cover to fall. No injuries have been reported.

Moderate·FDA·Apr 8, 2026

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.

Moderate·FDA·Mar 25, 2026

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.

Moderate·FDA·Feb 25, 2026

Stryker is recalling 2 products: certain MV3 bariatric beds and Arise 1000EX mattresses. The products were sold close together, suggesting they may be used together, but they have not been tested for compatibility and are not designed to be used as a combination.

Moderate·FDA·Dec 17, 20252 products

Stryker is recalling three NICO product lines: Myriad handpieces, Myriad illumination packs, and BrainPath Shephard's hooks. The packaging tape used to secure components contains latex, even though the products are labeled latex-free. Latex can cause an allergic reaction in people who are sensitive to it. No injuries have been reported.

Moderate·FDA·Dec 3, 20253 products

Due to manufacturing issue, reprocessed shears, may become stuck in the "on position" resulting in continuous activation.

FDA·Nov 19, 2025