Overview of recall records associated with Shire Human Genetic Therapies, Inc., including dates, categories and classifications where available.
Classification mix: Class I: 5.
Defective Delivery System: potential risk of rubber stopper particles clogging the needle and leading to underdosing
Defective Delivery System: potential risk of rubber stopper particles clogging the needle and leading to underdosing
Defective Delivery System: potential risk of rubber stopper particles clogging the needle and leading to underdosing
Defective Delivery System: potential risk of rubber stopper particles clogging the needle and leading to underdosing
Presence of Particulate Matter; Particulates identified as stainless steel and barium sulfate.
This page summarizes recall records in which the official source identifies Shire Human Genetic Therapies, 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.
