The pre-vacuum steam sterilization (wrapped method) temperature in the Instructions for Use incorrectly listed 121-123¿C , instead of the correct 132-133¿C.
Medical Devices Recalls
Medical equipment, implants, and diagnostic devices
Presource PBDS, Gyn Laparoscopy Kit, Circulator
Cardinal Health, Medical Products & Services
Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit that may contain outer plastic packaging on one or more components. If the packaging is removed without disassembling the components, remnants of the plastic from the packaging material may become lodged in the filter potentially causing an obstruction of airflow.
Presource PBDS, Total Hip, Kit, Circulator
Cardinal Health, Medical Products & Services
Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit that may contain outer plastic packaging on one or more components. If the packaging is removed without disassembling the components, remnants of the plastic from the packaging material may become lodged in the filter potentially causing an obstruction of airflow.
The pre-vacuum steam sterilization (wrapped method) temperature in the Instructions for Use incorrectly listed 121-123¿C , instead of the correct 132-133¿C.
DePuy Mitek Tissue Liberator -Blade Up Catalog Number: 214623 The Reusable Arthroscopy Instruments are reusable, non-powered surgical instruments used during arthroscopic surgery of any joint except the spine.
DePuy Mitek, Inc., a Johnson & Johnson
Labeled incorrectly as a Blade Up configuration instead of a Blade Down configuration.
Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
The pre-vacuum steam sterilization (wrapped method) temperature in the Instructions for Use incorrectly listed 121-123¿C , instead of the correct 132-133¿C.
The pre-vacuum steam sterilization (wrapped method) temperature in the Instructions for Use incorrectly listed 121-123¿C , instead of the correct 132-133¿C.
Unable to pass catheter through outer sheath during embryo transfer
The pre-vacuum steam sterilization (wrapped method) temperature in the Instructions for Use incorrectly listed 121-123¿C , instead of the correct 132-133¿C.
Unable to pass catheter through outer sheath during embryo transfer
Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
Increased levels of false positives in BD Probe Tech Neisseria gonorrhoeae Q Amplified DNA assay kits.
Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
Presource PBDS, Total Joint, Kit, Circulator
Cardinal Health, Medical Products & Services
Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit that may contain outer plastic packaging on one or more components. If the packaging is removed without disassembling the components, remnants of the plastic from the packaging material may become lodged in the filter potentially causing an obstruction of airflow.
Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
The pre-vacuum steam sterilization (wrapped method) temperature in the Instructions for Use incorrectly listed 121-123¿C , instead of the correct 132-133¿C.
Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
The pre-vacuum steam sterilization (wrapped method) temperature in the Instructions for Use incorrectly listed 121-123¿C , instead of the correct 132-133¿C.
The pre-vacuum steam sterilization (wrapped method) temperature in the Instructions for Use incorrectly listed 121-123¿C , instead of the correct 132-133¿C.