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All product recalls associated with Stryker Endoscopy.
Total Recalls
1000
Past Year
1000
Class I (Serious)
143
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.
The coupler on this device was manufactured without set-screws that are used to hold and center the rear assembly and the endobody. The coupler is part of the camera system and affects the ability to focus.
Contamination: The firm learned that up to 2.2% oversulfated chondroitin was found in a batch of crude heparin they received from their supplier.
Possible misdiagnosis or inappropriate treatment based on the image. Signal homogeneity may be affected when BRAVO applications are set with IR Prep off. The concern is that signal inhomogeneity can result in an erroneous diagnosis.
Software anomaly results in inaccurate information being printed out on the Delivery Report, even though the compounder performed the compounding correctly.
This recall involves Rock 'N Ride plush rocker toys sold in eight models: brown pony, pink pony, pink unicorn, deluxe pony, deluxe bull, lil' penguin, lil' propeller plane and Clifford big red rocker. The toys have molded plastic rocker bases and were sold for children at least 18 months old and up to 65 lbs. A button on the toy's ear, hat or dash activates songs and phrases when pressed. Rockers included in this recall have a date code from July 26, 2007 through December 29, 2007. The date codes are printed on a sticker inside the battery compartment.
The wood penguin-shaped toy has a black head with rubber fins, a yellow nose and a white body with red on the base. The toy is round-shaped and creates a soft bell jingle when spun. The toy measures about 3 ¾ inches in height and about 3 inches in diameter. "PLAN TOYS" and UPC number 084543521109 or EAN number 8854740052117 are printed on the outside of the packaging of the toy.
Medtronic has identified an issue with 685 Hall Easy-Fit valves Models A7700 and M7700 in which the holder of the valve was incorrectly secured to the valve. This could potentially make it difficult to easily disengage the holder from the valve.
This recall was initiated after the firm received several complaints reporting issues with deflection. The catheter may become caught in the mitral valve, requiring surgical procedures, valve may be torn while trying to dislodge, unable to retract the catheter through the sheath and require surgical intervention to remove, pulling on catheter to remove may lead to large atrial septal tear, and sep
This recall involves model year 2008 Rhino YXR450 and YXR700 Side-by-Side Vehicles as listed below: Make/Model Primary Identification Numbers 2008 Rhino 450 YXR45FX AJ32Y-001001 ~ 001598 YXR45FHX AJ30Y-000501 ~ 000897 YXR45FSPX AJ34Y-000201 ~ 000794 2008 Rhino 700FI YXR70FX AM16Y-000101 ~ 003000 YXR70FDUX AM20Y-000101 ~ 000700 YXR70FHX AM18Y-000101 ~ 000800 YXR70FSEPX/FSP2X AM23Y-000101 ~ 001000 YXR70FSPX AM21Y-000101 ~ 001200 The Primary Identification Number is stamped on the driver's side rear tire frame rail.
Reports received regarding disassembly of T-Handle Driver components during surgery dropping the closure top into the surgical site.
Reports received regarding disassembly of T-Handle Driver components during surgery dropping the closure top into the surgical site.
False Results: The product may exhibit falsely elevated results. The affected lots demonstrate sporadic variability in recovery of calibrator and quality control; therefore this issue may not be readily detected upon calibration or during routine processing of Quality Control.
Misbranded/mispackaged device was distributed. Product labeled to contain 72 inch Standard Drip ( IV) Administration Sets, actually contained 60 inch (IV) administration sets with a' Y' site.
Certain PANTA Nails from one lot were incorrectly manufactured. The internal thread for certain PANTA Nails (Part Number 500050ND; Lot Number: E7XX) may present an insufficient depth and may not allow the engagement of the threaded part of the compression device. The risks presented include: an increase in surgery time, or the implantation of a nail less ideally suited for the patient's anatomy
Unexpected movement of the X-ray table may occur. These movements may lead to patient injury, e.g., an uncontrolled tilt may cause the patient to slip off.
Wiring in battery back-up power supply may short and cause thermal damage to ventilator.
The heparin lock flush solution was manufactured from contaminated Heparin Sodium USP Active Pharmaceutical Ingredient (API). The FDA has received reports of serious injuries and/or deaths in patients administered finished heparin injectable products manufactured from heparin API containing this contaminant.
The heparin lock flush solution was manufactured from contaminated Heparin Sodium USP Active Pharmaceutical Ingredient (API). The FDA has received reports of serious injuries and/or deaths in patients administered finished heparin injectable products manufactured from heparin API containing this contaminant.
Hep-Lock Flush vials included in Integra's PICC Insertion Trays contain a heparin component that has been recalled by Baxter for contaminated heparin.
Discovery of the potential for Pin and Punch interference of the Size 3 Scorpio Notch Preparation Guide that may result in damage to bone if a user aggressively attempts to seat an obstructed punch.