Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 253–264 of 816 recalls
Due to products being released for distribution prior to completion of the required quality control release process the sterility assurance cannot be confirmed.
Due to probe bags that may have a compromised or incomplete sterile pouch seal.
The supplier manufactured anatomical left plates with an incorrect thread orientation.
The supplier manufactured anatomical left plates with an incorrect thread orientation.
Inflation device handle may detach from the syringe during procedure.
Inflation device handle may detach from the syringe during procedure.
Inflation device handle may detach from the syringe during procedure.
Inflation device handle may detach from the syringe during procedure.
Inflation device handle may detach from the syringe during procedure.
Inflation device handle may detach from the syringe during procedure.
Inflation device handle may detach from the syringe during procedure.
Needle free access device intended as accessory to vascular access used in hemodialysis or accessory to intravascular administration sets has a silicone seal which may bulge at the top, separate from the body, tear;…