Medical DeviceJun 24, 2020
Stryker End Cap T2 Humerus ¿6mm, 15mm height recall — FDA Z-2378-2020
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Class IIFDA: TerminatedStryker GmbH
Recall history in this database
Classification mix: Class II: 70.
Medical DeviceJun 24, 2020
Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x30 mm recall — FDA Z-2381-2020
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Class IIFDA: TerminatedStryker GmbH
Medical DeviceJun 24, 2020
Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x50 mm recall — FDA Z-2386-2020
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Class IIFDA: TerminatedStryker GmbH
Medical DeviceJun 24, 2020
Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x35 mm recall — FDA Z-2382-2020
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Class IIFDA: TerminatedStryker GmbH
Medical DeviceJun 24, 2020
Stryker Locking Screw, Fully Threaded S2 05x35 mm recall — FDA Z-2373-2020
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Class IIFDA: TerminatedStryker GmbH
Medical DeviceJun 24, 2020
Stryker End Cap, Standard T2 Humerus ¿6 mm recall — FDA Z-2376-2020
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Class IIFDA: TerminatedStryker GmbH
Medical DeviceJun 24, 2020
Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x45 mm recall — FDA Z-2385-2020
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Class IIFDA: TerminatedStryker GmbH
Medical DeviceJan 15, 2020
Stryker T2 Alpha Delta Strike Plate IMN Instruments - part of the IMN Instruments System and recall — FDA Z-0780-2020
Instrument can break at the level of the thread when being exposed to high forces during nail implantation or removal which can lead to complications during nail insertion and removal.
Class IIFDA: TerminatedStryker GmbH
Medical DeviceJan 15, 2020
Stryker Pin To Rod Coupling External Fixation System Hoffmann II Compact - Pin To Rod recall — FDA Z-0781-2020
Pin To Rod Coupling could not clamp the pin and rod as intended
Class IIFDA: TerminatedStryker GmbH
Medical DeviceSep 4, 2019
Stryker GmbH Endotrig ETF Hook Blade, Catalog Number 1052-1 The EPF system is designed for recall — FDA Z-2412-2019
The seal integrity of the sterile bag containing the kits may be compromised.
Class IIFDA: TerminatedStryker GmbH
Medical DeviceSep 4, 2019
Stryker GmbH Endotrac EPF/EGR Hook Blade, Catalog Number 3055-1 The EPF system is designed recall — FDA Z-2418-2019
The seal integrity of the sterile bag containing the kits may be compromised.
Class IIFDA: TerminatedStryker GmbH
Medical DeviceSep 4, 2019
Stryker GmbH Endotrac EPF/EGR Push Blade, Catalog Number 3053-1 The EPF system is designed recall — FDA Z-2416-2019
The seal integrity of the sterile bag containing the kits may be compromised.
Class IIFDA: TerminatedStryker GmbH
Medical DeviceSep 4, 2019
Stryker GmbH Endintrak 2 Hook Blade, Catalog Number 4058-1 The EPF system is designed for recall — FDA Z-2419-2019
The seal integrity of the sterile bag containing the kits may be compromised.
Class IIFDA: TerminatedStryker GmbH
Medical DeviceSep 4, 2019
Stryker GmbH Endotrac EPF/EGR Triangle Blade, Catalog Number 3054-1 The EPF system is recall — FDA Z-2417-2019
The seal integrity of the sterile bag containing the kits may be compromised.
Class IIFDA: TerminatedStryker GmbH
Medical DeviceSep 4, 2019
Stryker GmbH Endotrac EPF/EGR Hook Blade, Angled, Catalog Number 3055A-1 The EPF system is recall — FDA Z-2423-2019
The seal integrity of the sterile bag containing the kits may be compromised.
Class IIFDA: TerminatedStryker GmbH
Medical DeviceSep 4, 2019
Stryker GmbH Endintrak 2 Hook Blade, Angled, Catalog Number 4058A-1 The EPF system is recall — FDA Z-2424-2019
The seal integrity of the sterile bag containing the kits may be compromised.
Class IIFDA: TerminatedStryker GmbH
Medical DeviceSep 4, 2019
Stryker GmbH Endotrac ECTR Push Blade, Catalog Number 2053-1 The EPF system is designed for recall — FDA Z-2413-2019
The seal integrity of the sterile bag containing the kits may be compromised.
Class IIFDA: TerminatedStryker GmbH
Medical DeviceSep 4, 2019
Stryker GmbH Endotrac ECTR Triangle Blade, Catalog Number 2054-1 The EPF system is designed recall — FDA Z-2414-2019
The seal integrity of the sterile bag containing the kits may be compromised.
Class IIFDA: TerminatedStryker GmbH
Medical DeviceSep 4, 2019
Stryker GmbH Endotrac ECTR Hook Blade, Catalog Number 2055-1 The EPF system is designed for recall — FDA Z-2415-2019
The seal integrity of the sterile bag containing the kits may be compromised.
Class IIFDA: TerminatedStryker GmbH
Medical DeviceSep 4, 2019
Stryker GmbH Endotrac EPF/EGR Triangle Blade, Angled, Catalog Number 3054A-1 The EPF system recall — FDA Z-2422-2019
The seal integrity of the sterile bag containing the kits may be compromised.
Class IIFDA: TerminatedStryker GmbH
Medical DeviceSep 4, 2019
Stryker GmbH Endotrac ECTR Hook Blade, Angled, Catalog Number 2055A-1 The EPF system is recall — FDA Z-2421-2019
The seal integrity of the sterile bag containing the kits may be compromised.
Class IIFDA: TerminatedStryker GmbH
Medical DeviceSep 4, 2019
Stryker GmbH Endotrac ECTR Triangle Blade, Angled, Catalog Number 2054A-1 The EPF system is recall — FDA Z-2420-2019
The seal integrity of the sterile bag containing the kits may be compromised.
Class IIFDA: TerminatedStryker GmbH
Medical DeviceNov 7, 2018
Stryker GmbH Hoffman LRF Hexapod Strut, Extra Short 183mm-295mm, Model Number 4935-0-040 recall — FDA Z-0291-2019
The press fit connection of the Angular Sleeve and pin of the U-Joint and Click Lock did not meet specification. A dimensional discrepancy of the bore hole of the Angular Sleeve may cause a…
Class IIFDA: TerminatedStryker GmbH
Medical DeviceNov 7, 2018
Stryker GmbH Hoffman LRF Hexapod Strut, Extra Short 105mm-139mm, Model Number 4935-0-020 recall — FDA Z-0289-2019
The press fit connection of the Angular Sleeve and pin of the U-Joint and Click Lock did not meet specification. A dimensional discrepancy of the bore hole of the Angular Sleeve may cause a…
Class IIFDA: TerminatedStryker GmbH
Understanding this recall history
This page summarizes recall records in which the official source identifies Stryker GmbH as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.