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All product recalls associated with Stryker Spine.
Total Recalls
1000
Past Year
731
Class I (Serious)
175
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Product dissembled in the tray or prior to being loaded onto the inserter or tightening on the rod
The material may solidify in the bottle, and thus be rendered unusable.
Need to modify the closing speed of the shielding doors in the event of an emergency exit
Data generation error: If the cytosettings is not refreshed or restarted during data importation, the output will include old and new data.
This recall involves Lasko ceramic heaters manufactured in 2005. Model numbers included in the recall are: 5132, 5345, 5362, 5364, 5420, 5532, 5534 and 5566. Model numbers are located on the bottom of the unit or at the rear of the base of the heaters.
Complaints received indicating open seals on blister paks, potentially compromising the sterility of the product.
The recalled dishwashers include the ASKO model series DW95 with model numbers 1355, 1385, 1475, 1485, 1555, 1585, 1595, 1655, 1805, 1885, and 1895, manufactured from January 1995 through April 2000. The model number, serial numbers and manufacture date are printed on the name plate on the right interior side of the dishwasher door. Asko dishwashers manufactured after April 2000 are not included in the recall.
Sling bar may have a center bolt break at the adapter while in use
Sling bar may have a center bolt break at the adapter while in use
Model J Series dry fire sprinklers come in pendent, upright, and sidewall configurations. The name "Globe," the letter "J" and the year of manufacture (1990 though 1999) are embossed on the frame of each sprinkler. These dry sprinklers were designed to be installed in areas of buildings where the sprinklers or water supply pipes may be subject to freezing, such as unheated attics, freezers and coolers, parking garages, porches and warehouses.
Lack of assurance of sterility, in that the product is labeled as sterile but the package may not have been sealed.
Target Alignment Error : A mechanical component/software incompatibility caused by a specific combination of the BrainLAB Target Positioner version 40700-3A for Leksell headrings and BrainLAB planning software resulted in a 1.25 mm shift in target area alignment during radiosurgery treatment.
The tubes may kink during use which may impede or prevent ventilation.
There has been an issue with "Image Fushing" where low precision calculation caused images to become inaccurate.
Stryker Orthopaedics became aware that Trident Hemispherical Shells, Catalog Number 508-11-74J, are actually marked and labeled as Catalog Number 598-11-72J, Lot Code 20282301
This recall involves toy sets with multiple action figures and vehicles. The model number (88931), Universal Product Code (6 98567 88931 4) and Soldier Bear logo are printed on the product's packaging. The backs of the action figures are marked with letters "TC-ST."
Sporadic absolute count recovery failures with assayed control cell products when using Lot Number 754801F of the Flow-Count Fluorospheres. Additionally, this lot has experienced secondary fluorescent populations containing more than 20% of the total population, as stated in the Evidence of Deterioration section of the Package Insert.
Defective component (power supply)
Incompatible components: The Finger Clip Sensors - with a Serial Number prefix of PA514, PA515, YE508, ZC502 and ZG512 - are missing an additional diode and higher resistor in its existing configuration making them inoperable when used to interface with those Ohmeda Tuffsat monitors previously re-configured by Ohmeda to include a detection circuit for diodes.
Mislabeling : box and bag labels are incorrectly labeled to indicate the product contains Sodium Fluoride/Potassium Oxalate, however the instructions for use and the product itself are correct in the additive indicated and used (Sodium Fluoride/Na2EDTA).