Manufacturer
75 recalls in our database name Stryker GmbH as the manufacturing or recalling firm.
Of the 75 recalls from Stryker GmbH we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 19 (25%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Stryker GmbH is recalling 17 T2 Basic Long Instrument Sets because faceplates may incorrectly identify them as T2 Basic Short sets.
Stryker GmbH is recalling 832 Hoffman LRF Hexapod Struts because a manufacturing defect may cause the pin to displace, compromising the stability of the orthopedic frame.
Stryker GmbH is recalling 578 Hoffmann LRF Hexapod Struts because a manufacturing defect may cause the pin to displace, compromising the stability of the orthopedic frame.
Stryker GmbH is recalling 867 Hoffman LRF Hexapod Struts because a manufacturing defect may cause the pin to displace, compromising the stability of the medical device.
Stryker GmbH is recalling 1,355 Hoffman LRF Hexapod Struts because a manufacturing defect may cause the pin to displace, compromising frame stability.
Stryker GmbH is recalling 233 units of Hoffmann LRF Hexapod Software because it may compute erroneously accelerated correction plans under specific settings.
Stryker GmbH is recalling 38 T2 orthopedic nails due to incomplete Tyvek lid seals that may compromise sterility.
Stryker GmbH is recalling 17 femoral nails because non-conforming cannulation may reduce component strength and cause premature breakage.
Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce component strength and lead to premature breakage.
Stryker GmbH is recalling seven femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.
Stryker GmbH is recalling specific ankle arthrodesis nails because non-conforming cannulation may reduce strength and cause premature breakage.
Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce component strength and lead to premature breakage.
Stryker GmbH is recalling two femoral nails that may have non-conforming cannulation, potentially leading to reduced strength and premature breakage.
Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.
Stryker GmbH is recalling specific femoral nails due to potential manufacturing defects that could cause the device to break prematurely.
Stryker GmbH is recalling specific Tibial Nails because non-conforming cannulation may reduce strength and cause premature breakage.
Stryker GmbH is recalling specific femoral nails due to potential manufacturing defects that could cause the device to break prematurely.
Stryker GmbH is recalling specific ankle arthrodesis nails because non-conforming cannulation may reduce strength and cause premature breakage.
Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.
Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.
Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.
Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce component strength and cause premature breakage.
Stryker GmbH is recalling nine femoral nails because non-conforming cannulation may reduce component strength and cause premature breakage.
Stryker GmbH is recalling Farabeuf Clamps for 3.5mm Screws PRO because laser etching indicating compression or distraction mode is on the wrong side of the lever arm.
Stryker GmbH is recalling 18 Hinge Coupling Hoffmann LRF units because connecting nuts were incorrectly packed in hinge coupling packaging.