Valorem Surgical PALLAS M/MAXIMIS Poly Screw 6.5 x 40mm recall — FDA Z-2936-2017
Devices are not consistent with Quality System Requirements.
Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Insufficient documentation to support product sterility claims.
Insufficient documentation to support product sterility claims.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Insufficient documentation to support product sterility claims.
Insufficient documentation to support product sterility claims.
Devices are not consistent with Quality System Requirements.
Insufficient documentation to support product sterility claims.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Insufficient documentation to support product sterility claims.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Insufficient documentation to support product sterility claims.
Insufficient documentation to support product sterility claims.
Devices are not consistent with Quality System Requirements.
Insufficient documentation to support product sterility claims.
Insufficient documentation to support product sterility claims.
Browse recent months with enough recall history for useful comparison.