Overview of recall records associated with Argon Medical Devices, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 30, Class I: 3.
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
This page summarizes recall records in which the official source identifies Argon Medical Devices, 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.
