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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

350

Past Year

Class I (Serious)

Most Recent

Nov 2025

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 201–220 of 350 recalls

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 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

1...9 101112 13...18

Page 11 of 18Next

Class I

High

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

GETINGE US SALES LLC: The HEMASHIELD PLATINUM Woven Double Velour Vascular Graf...

Based on an internal incident report, Getinge/Intervascular SAS has identified that the one (1) HEMASHIELD GOLD Knitted Microvel Double Velour Vascular Bifurcated Graft product with the diameter size of 16 x 9 mm is likely incorrectly packed inside of the carton which was labeled to contain a HEMASHIELD PLATINUM Woven Double Velour Vascular Graft product with the diameter size of 16 x 8 mm ((REF: M00202166168P0, Lot: 18K31, SN: 1190443415, size 16 x 8 mm).

FDAAug 22, 2019NJ• GETINGE US SALES LLC

GETINGE US SALES LLC: Getinge MCC Flow i Disposable CO2 absorber, used in anest...

Reversed expiration and manufacturing date on the label

FDAJul 22, 2019Nationwide• GETINGE US SALES LLC

Skeletal Kinetics, Llc: OsteoVation, Inject Bone Filler Kits, 5cc (part number 39...

A discrepancy was found between the Mixing Instruction Card and the Instructions for Use for the 5cc and 10 cc bone void filler kits. No customer complaints or reports of injury have been received.

FDAJun 6, 2019Nationwide• Skeletal Kinetics, Llc

GETINGE US SALES LLC: PulsioFlex Monitoring System, Part Number: 6882747, Model...

The monitor displays an error message . The error message states "internal error restart or service".

FDAJun 5, 2019Nationwide• GETINGE US SALES LLC