Overview of recall records associated with Merit Medical Systems, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 101, Class I: 5.
Vertebral hydraulic assemblies has incorrect expiration date printed on the labels.The product's shelf-life is two (2) years, but the expiration date printed on the labels is five (5)…
labeling error: Due to a manufacturing issue, product package was incorrectly labeled with the incorrect sheath size and the incorrect sheath assembly was included in the product packaging.…
During the sterilization of radial compression devices, some of the inflatable balloons may break or burst, which may result in air leakage and the inability to maintain…
A nonsterile bulk product designated for further processing in a tray was inadvertently shipped to a customer.
Labeling error; It was identified that a Procedure Kit/Tray contained incorrect latex labeling information (i.e. indicated Latex Free)
Labeling error; It was identified that a Procedure Kit/Tray contained incorrect latex labeling information (i.e. indicated Latex Free)
Supplier manufacturing defect with the syringe plunger tip.
Mix-up between adult and pediatrics PD catheter.
2 Cuff catheters were incorrectly configured and labeled as 1 Cuff product and placed into these dialysis kits.
1 Cuff catheters were incorrectly configured and labeled as 2 Cuff product and placed into these dialysis kits.
This page summarizes recall records in which the official source identifies Merit Medical Systems, Inc. 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.
