Stryker recall — FDA Z-1508-2020
Potential diff. in the length of the sheath tube and the sheath/probe. A diff. in length could lead to the base of the sheath/probe not being fully seated in the sheath tube which could…
Overview of recall records associated with Stryker Corporation, including dates, categories and classifications where available.
Classification mix: Class II: 108.
Potential diff. in the length of the sheath tube and the sheath/probe. A diff. in length could lead to the base of the sheath/probe not being fully seated in the sheath tube which could…
There is a potential problem with firm s Connected OR Cart, 120V resulting in cart monitor not attaching flush with their monitor stow handle. The product is not manufactured to…
Complaints have been received regarding difficulty in removing the driver from the screw. High driver removal forces can lead to the screw pulling out still attached to the driver. This…
Complaints have been received regarding difficulty in removing the driver from the screw. High driver removal forces can lead to the screw pulling out still attached to the driver. This…
The heated tube sets were consistently leaking and detaching from the cassette.
The heated tube sets were consistently leaking and detaching from the cassette.
The heated tube sets were consistently leaking and detaching from the cassette.
Inadvertent shipment of expired units.
The recalled products were shipped without the required temperature control packaging, therefore could potentially have been exposed to elevated temperatures during transit.
Routine bioburden testing of certain lots were found to have levels higher than internal acceptable rates.
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…
Routine bioburden testing of certain lots were found to have levels higher than internal acceptable rates.
This page summarizes recall records in which the official source identifies Stryker Corporation 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.