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Shire Human Genetic Therapies, Inc.

Shire Human Genetic Therapies, Inc. Recalls

All product recalls associated with Shire Human Genetic Therapies, Inc..

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Sep 2019

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–5 of 5 recalls

Natpara 25 mcg (Shire) – Delivery System Defect (2019)

Defective Delivery System: potential risk of rubber stopper particles clogging the needle and leading to underdosing

Class IHigh

FDASep 12, 2019Nationwide• Shire Human Genetic Therapies, Inc.

Natpara 100 mcg (Shire) – Delivery System Risk (2019)

Defective Delivery System: potential risk of rubber stopper particles clogging the needle and leading to underdosing

Class IHigh

FDASep 12, 2019Nationwide• Shire Human Genetic Therapies, Inc.

Natpara Injection (Shire) – Delivery System Defect (2019)

Defective Delivery System: potential risk of rubber stopper particles clogging the needle and leading to underdosing

Class I

High

FDASep 12, 2019Nationwide• Shire Human Genetic Therapies, Inc.

Natpara Injection (Shire) – Delivery System Defect (2019)

Defective Delivery System: potential risk of rubber stopper particles clogging the needle and leading to underdosing

Class IHigh

FDASep 12, 2019Nationwide• Shire Human Genetic Therapies, Inc.

VPRIV Injection 400 Units (Shire) – Particulate Contamination (2014)

Presence of Particulate Matter; Particulates identified as stainless steel and barium sulfate.

Class IHigh

FDAMar 14, 2014Nationwide• Shire Human Genetic Therapies, Inc.