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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

1000

Past Year

589

Class I (Serious)

Most Recent

Jan 2026

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 4801–4820 of 10393 recalls

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.

Wintergreen Essential Oil (Healing Solutions) – Packaging issue (2019)

This recall includes all 10-, 30- and 60-mililiter amber glass bottles of wintergreen and birch essential oils sold prior to April 15, 2019. The label on each bottle displays the name of the product-Wintergreen or Birch-"100% Pure Therapeutic Grade Essential Oil," and the size of the container.

Low

CPSCSep 10, 2019Nationwide• Healing Solutions LLC, of Phoenix, Ariz.

Stormrider Air Rifle (DIANA) – Discharge risk (2019)

This recall involves the DIANA Stormrider Gen 2 Air Rifle with 2-stage adjustable trigger. The recalled products are .177 and .22 caliber, pre-charged pneumatic air rifles that are powered by a compressed air cylinder. "DIANA Stormrider" as well as the caliber and serial number are printed on each affected air rifle. Air rifles with the following item and serial numbers are included in the recall: Recalled DIANA Stormrider Gen 2 Air Rifles Item Numbers 1900001 & 1900101 Serial Numbers 2318220145032949E - 2318229955034368E 2318229955075924I - 2318229955076323I

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Very High

CPSCSep 10, 2019Nationwide• Shaoxing Snowpeak Air Gun Factory, of China

HeartStart HS1 AED (Philips) – Circuit Assembly Issue (2019)

Affected devices contain a Printed Circuit Assembly (PCA) that was not manufactured/repaired in accordance to quality standards.

Moderate

FDASep 10, 2019CA, CT, FL +10 more• Philips North America LLC

HeartStart FRx AED (Philips) – Circuit Assembly Issue (2019)

Affected devices contain a Printed Circuit Assembly (PCA) that was not manufactured/repaired in accordance to quality standards.

Moderate

FDASep 10, 2019CA, CT, FL +10 more• Philips North America LLC

Brain Charge Supplement (Source Naturals) – Labeling error (2019)

Labeling error; incorrect supplement facts panel and label claims for two ingredients were lower than the product formulation.

Class IIILow

FDASep 10, 2019AL, AZ, CA +27 more• Threshold Enterprises Ltd

Rosa Brain 3.0 (MEDTECH) – Surgical Instrument Placement (2019)

The instrument holder may be sent on a trajectory that is not within the intended target. If it is not corrected, the associated device may be placed incorrectly.

Moderate

FDASep 10, 2019Nationwide• MEDTECH SAS 900 Rue Du Mas De Verchant Montpellier France

Frozen Yellowfin Tuna (Truong Phu Xanh) - Elevated Histamine Levels (2019)

Elevated histamine levels.

Class IIModerate

FDASep 10, 2019CA, FL, NJ +1 more• Truong Phu Xanh Co.,

Nucala (Cardinal Health) - temperature storage issue (2019)

Temperature Abuse; Product stored and shipped outside of labeled storage requirements.

Class IIModerate

FDASep 6, 2019Nationwide• Cardinal Health dba Specialty Pharmaceutical Services

PolyCut Mowing Heads (STIHL) - Injury Hazard (2019)

Laceration Risk

This recall involves mowing head cutting attachments compatible with some models of STIHL-brand trimmers, brushcutters, and clearing saws. The mowing heads can be identified by the name "STIHL" and model number "27-3" or "47-3" located on the original packaging and molded on the top side of the mowing head. The mowing heads have three orange plastic blades, each attached with a bolt and a nut, a black top housing, and a white bottom housing.

Moderate

CPSCSep 5, 2019Nationwide• STIHL Incorporated, of Virginia Beach, Va.

Achilles Insight Bone Sonometer (GE Healthcare) – Power Cord Compatibility (2019)

Certain Achilles Express and Achilles Insight systems were shipped with European CEE-7/7 Type Power Cords to countries where three protruding pin plugs are required for protective earth connection.

High

FDASep 3, 2019Nationwide• GE Healthcare, LLC