Stryker Recalls
192 recalls on record · May 18, 2016 to August 12, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
August 12, 2026Medical DevicesFDA
Stryker Corporation recalls STRYKER PKG., STRYKEFLOW SUCTION/IRRIGATOR PS, Catalog Number 0250070540
Hazard: There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
August 12, 2026Medical DevicesFDA
Stryker Corporation recalls STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530
Hazard: There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
August 12, 2026Medical DevicesFDA
Stryker Corporation recalls STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0250070640
Hazard: There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
August 12, 2026Medical DevicesFDA
Stryker Corporation recalls STRYKER AHTO TUBE SET WITH TIP PACKAGING, Catalog Number 0250070620
Hazard: There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
August 12, 2026Medical DevicesFDA
Stryker Corporation recalls STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600
Hazard: There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
August 5, 2026Medical DevicesFDA
Stryker GmbH recalls Stryker Hoffmann II Connecting Rod Micro 3 x 150mm. Catalog Number: 50796150.
Hazard: Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
August 5, 2026Medical DevicesFDA
Stryker GmbH recalls Stryker Hoffmann II Connecting Rod Micro 3 x 120mm. Catalog Number: 50796120.
Hazard: Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
August 5, 2026Medical DevicesFDA
Stryker GmbH recalls Stryker Hoffmann II Connecting Rod Micro 3 x 90mm. Catalog Number: 50796090.
Hazard: Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
August 5, 2026Medical DevicesFDA
Stryker GmbH recalls Stryker Hoffmann II Connecting Rod Micro 3 x 60mm. Catalog Number: 50796060.
Hazard: Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
August 5, 2026Medical DevicesFDA
Stryker GmbH recalls Stryker Hoffmann II Connecting Rod Micro 3 x 50mm. Catalog Number: 50796050.
Hazard: Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
August 5, 2026Medical DevicesFDA
Stryker GmbH recalls Stryker Hoffmann II Connecting Rod Micro 3 x 40mm. Catalog Number: 50796040.
Hazard: Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
August 5, 2026Medical DevicesFDA
Stryker GmbH recalls Stryker Hoffmann II Connecting Rod Micro 3 x 30mm. Catalog Number: 50796030.
Hazard: Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
June 10, 2026Medical DevicesFDA
Stryker Corporation recalls Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
Hazard: It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being shipped to your facility. There is a potential risk of electrical shock due to the device s safety testing being unverifiable.
May 20, 2026Medical DevicesFDA
Stryker Corporation recalls Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube Sets are intended to
Hazard: Due to nonconforming products being inadvertently distributed.
February 25, 2026Medical DevicesFDA
Stryker Corporation recalls MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN): 008500
Hazard: Due to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target tissue removal procedures.
December 3, 2025Medical DevicesFDA
Stryker Corporation recalls NICO BrainPath; Product Number/Product Name NN-8024 BrainPath Shephard's Hook - Greenberg; NN-8025 BrainPath Shep
Hazard: Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.
December 3, 2025Medical DevicesFDA
Stryker Corporation recalls NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination Sleeve/Fiber; Product No. NN-1001 13g Illuminat
Hazard: Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.
December 3, 2025Medical DevicesFDA
Stryker Corporation recalls NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP; NN-8001 15x 13 MHP; NN-8002 15x 25 MHP
Hazard: Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.
August 13, 2025Medical DevicesFDA
Stryker Corporation recalls Stryker SmartPump Tourniquet, disposable sterile (single use) DISP 18X3,1BLA,1PRT QUICK / 5921-018-135; DISP 18X3
Hazard: Tourniquet cuff flange may become detached from the bladder. If leak occurs during the procedure, there may be risk of hemorrhage, resulting in blood loss greater than expected. Other serious risks include cerebral hypotension and cardiovascular collapse and arrest, risking stroke or death. Specific to IVRA, patient toxicity may also occur due to rapid systemic absorption of anesthetics.
July 30, 2025Medical DevicesFDA
Stryker Corporation recalls Stryker, StrykeFlow REF: 0250070520 / 2, Disposable Suction/Irrigator with Disposable Tip
Hazard: Due to complaints their is the potential that irrigation solution may leaked into the handpiece and battery pack causing it to malfunction.
July 30, 2025Medical DevicesFDA
Stryker Corporation recalls Stryker, StrykeFlow , REF: 0250070500, 2, Disposable Suction/Irrigator without Disposable Tip
Hazard: Due to complaints their is the potential that irrigation solution may leaked into the handpiece and battery pack causing it to malfunction.
June 18, 2025Medical DevicesFDA
Stryker GmbH recalls Femoral Nail, RIGHT T2 GTN 8x300 mm. Catalog Number: 1851-0830S.
Hazard: Investigation determined that one lot of the T2 Greater Trochanter Nail (GTN) was labeled as left version but contained a right nail and another lot was labeled as right version but contained a left nail.
June 18, 2025Medical DevicesFDA
Stryker GmbH recalls Femoral Nail, LEFT T2 GTN 8x300 mm. Catalog Number: 1850-0830S.
Hazard: Investigation determined that one lot of the T2 Greater Trochanter Nail (GTN) was labeled as left version but contained a right nail and another lot was labeled as right version but contained a left nail.
June 18, 2025Medical DevicesFDA
Stryker GmbH recalls Long Nail, RIGHT Gamma4 10x320mm x 125, component of the Gamma4 System. Catalog Number: 84250320S.
Hazard: Investigation confirmed that the GAMMA4 Right Long Nail was manufactured with the geometry of a left nail.
April 23, 2025Medical DevicesFDA
Stryker GmbH recalls Guide Wire with Ruler Tube 3x1000 mm DIA; Catalog number/REF: 2351-3100S;
Hazard: The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.
April 23, 2025Medical DevicesFDA
Stryker GmbH recalls Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;
Hazard: The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.
April 9, 2025Medical DevicesFDA
Stryker Corporation recalls Hemopore 2PK nasal/sinus temporary wound dressing, Catalog Number 5400-222-208S
Hazard: There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
April 9, 2025Medical DevicesFDA
Stryker Corporation recalls Nasopore 4cm Standard 2PK fragmentable nasal dressing, Catalog Number 5400-212-004S and Nasopore 4cm Firm 2PK Catalog Nu
Hazard: There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
April 9, 2025Medical DevicesFDA
Stryker Corporation recalls Nasopore 4cm Standard 2PK fragmentable nasal dressing, Catalog Number 5400-212-004S and Nasopore 4cm Firm 2PK Catalog Nu
Hazard: There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
April 9, 2025Medical DevicesFDA
Stryker Corporation recalls Nasopore Ex Firm 8cm fragmentable nasal dressing, Catalog Number 5400-030-008 and Nasopore Forte plus 8cm Catalog Number
Hazard: There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.