Pyng Medical MATResponder Tourniquet recall — FDA Z-0228-2016
Once tested, it is required that the tourniquet be returned to its Ready position then placed in its packaging. Each tourniquet was tested for functionality, but in some cases, the…
Overview of recall records associated with Pyng Medical Corporation, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Once tested, it is required that the tourniquet be returned to its Ready position then placed in its packaging. Each tourniquet was tested for functionality, but in some cases, the…
This page summarizes recall records in which the official source identifies Pyng Medical Corporation 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.