Stryker Corporation: 46 recalls on record

Recalls filed with 1 agency: FDA (46).

First recall on record: May 18, 2016. Most recent: August 12, 2026.

Risk classification: Class II: 46

Most recent recalls

DateAgencyProduct
September 4, 2024FDAStryker iBur 4.0mm Precision Round, Distal Bend- intended to cut bone in the following m…Z-2723-2024
September 4, 2024FDAStryker iBur 3.0mm Diamond Match Head, Distal Bend - intended to cut bone in the followi…Z-2730-2024
September 4, 2024FDAStryker iBur 3.0mm Precision Round, Distal Bend- Intended to cut bone in the following m…Z-2722-2024
September 4, 2024FDAStryker iBur 3.0mm Precision Match Head, Distal Bend- intended to cut bone in the follo…Z-2731-2024
September 4, 2024FDAStryker iBur 2.0mm Diamond Round, Distal Bend- intended to cut bone in the following man…Z-2724-2024
September 4, 2024FDAStryker iBur 3.0mm Diamond Round, Distal Bend - intended to cut bone in the following ma…Z-2725-2024
September 4, 2024FDAStryker iBur 4.0mm Diamond Round, Distal Bend- intended to cut bone in the following man…Z-2726-2024
September 4, 2024FDAStryker iBur 3.0mm Coarse Diamond Round, Distal Bend - intended to cut bone in the follo…Z-2727-2024
September 4, 2024FDAStryker iBur 4.0mm Coarse Diamond Round, Distal Bend - intended to cut bone in the follo…Z-2728-2024
July 10, 2024FDACurved, super elastic cement delivery needle that passes through the cannula in a straigh…Z-2260-2024
July 10, 2024FDAThe Non-Sterile Flyte hood covers the user s head and neck region and is intended to be w…Z-2259-2024
July 10, 2024FDAThis product is a single use sterile device that is used to direct the lesion to the targ…Z-2261-2024
November 15, 2023FDADisposable Spetzler-Malis Bipolar forceps, 18CM SM DISP BAYONET 0.5MM TIP, Catalog Number…Z-0239-2024
September 27, 2023FDAStryker ACM (Advanced Cement Mixing) System: Break-Away Femoral Nozzle-, Allows the user…Z-2596-2023
April 12, 2023FDAStryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 30X4,1BLA,1PRT QUICK …Z-1339-2023
February 19, 2020FDAStryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Single, REF 3910-500-471, UDI 07613…Z-1148-2020
June 12, 2019FDAStryker High Flow II Tube Set, REF 0620-040-660, an accessory to the PNEUMO SURE High Fl…Z-1726-2019
June 13, 2018FDA3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Di…Z-2057-2018
March 14, 2018FDASTRYKER WEDGE INTERFERENCE SCREW SYSTEM, ACL Interface Screw, 9MM X 25MM, Model 023401005…Z-0837-2018
June 15, 2016FDAStryker FlowPort II Adapter: Model number: 00CAT00778 The FlowPort II Adapter is intend…Z-1910-2016
May 18, 2016FDACinchLock SS Knotless Anchor with Inserter; Model number CAT02462; Orthopedic: The …Z-1634-2016

Questions about this company

How many recalls does Stryker Corporation have?
Recalert has 46 U.S. recalls on record for Stryker Corporation, published between May 18, 2016 and August 12, 2026.
Which agencies have handled Stryker Corporation recalls?
Stryker Corporation appears as the recalling firm in recalls from: FDA (46).

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