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.
July 18, 2018Medical DevicesFDA
Stryker GmbH recalls Tibial Nail, Standard T2 Tibia ¿12x315 mm, Product Number 18221231S
Hazard: The manufacturer has discovered that potentially out-of-specification products may have left the factory. Non-conforming cannulation of the nails may result in reduced component strength and potentially premature nail breakage.
June 27, 2018Medical DevicesFDA
Stryker GmbH recalls Farabeuf Clamp for 3.5mm Screws PRO, Catalog # 705463
Hazard: Laser etching which indicates whether the device is in compression or distraction mode appears to be on the wrong side of the lever arm
June 13, 2018Medical DevicesFDA
Stryker Corporation recalls 3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Disposable Cannula device is desi
Hazard: Inadvertent shipment of expired units.
May 2, 2018Medical DevicesFDA
Stryker GmbH recalls Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of fractures, joint contractures, fusions, lim
Hazard: The wrong parts were picked for packaging. The connecting Nuts were packed in the packaging labeled with Hinge coupling
March 21, 2018Medical DevicesFDA
Stryker Corporation recalls CMI (Collagen Meniscus Implant) device, Ivy Sports Medicine s collagen-based meniscus implant Product Usage: The CMI
Hazard: The recalled products were shipped without the required temperature control packaging, therefore could potentially have been exposed to elevated temperatures during transit.
March 14, 2018Medical DevicesFDA
Stryker Corporation recalls ACL DISPOSABLE PACK BONE-TENDON-BONE, Model 0234020280, labeled sterile.
Hazard: Routine bioburden testing of certain lots were found to have levels higher than internal acceptable rates. It is indicated to be a single surgery use, disposable set of instrumentation for anterior cruciate ligament (ACL) reconstruction surgeries.
March 14, 2018Medical DevicesFDA
Stryker Corporation recalls STRYKER WEDGE INTERFERENCE SCREW SYSTEM, ACL Interface Screw, 9MM X 25MM, Model 0234010056, labeled sterile.
Hazard: Routine bioburden testing of certain lots were found to have levels higher than internal acceptable rates.
March 14, 2018Medical DevicesFDA
Stryker Corporation recalls STRYKER CASSETTE PUMP, AHTO Tube Set, labeled sterile. Includes the following: a. Stryker AHTO Tube Set Packaging (M
Hazard: Routine bioburden testing of certain lots were found to have levels higher than internal acceptable rates.
March 14, 2018Medical DevicesFDA
Stryker Corporation recalls StrykeFlow 2 System, labeled sterile. Includes the following: a. STRYKER LAPAROSCOPIC SUCTION IRRIGATOR, Suction/Irr
Hazard: Routine bioburden testing of certain lots were found to have levels higher than internal acceptable rates.
June 15, 2016Medical DevicesFDA
Stryker Corporation recalls Stryker FlowPort II Adapter: Model number: 00CAT00778 The FlowPort II Adapter is intended to connect the FlowPort II C
Hazard: Complaints were received for the Stryker FlowPort II Adapter, and investigation found that the scope sat in the adapter 180 degrees in the wrong direction
May 18, 2016Medical DevicesFDA
Stryker Corporation recalls CinchLock Flex Knotless Anchor with Inserter; Model number CAT02643; Orthopedic: The Pivot CinchLock SS Knotless An
Hazard: Stryker Endoscopy is recalling the CinchLock SS Knotless Anchor with Inserter and the CinchLock Flex Anchor with Inserter after 13 reports of an internal wire breaking upon deployment of the anchor.
May 18, 2016Medical DevicesFDA
Stryker Corporation recalls CinchLock SS Knotless Anchor with Inserter; Model number CAT02462; Orthopedic: The Pivot CinchLock SS Knotless Anc
Hazard: Stryker Endoscopy is recalling the CinchLock SS Knotless Anchor with Inserter and the CinchLock Flex Anchor with Inserter after 13 reports of s of an internal wire breaking upon deployment of the anchor.