RecallRadar

FDA Drug recall D-0037-2020

Natpara (parathyroid hormone) for Injection, 75 mcg, 2 pack medication cartridges, Rx only, For subcutaneous use only, Manufactured for: Sh…

On 2019-10-02 the FDA classified a Class I recall of Natpara (parathyroid hormone) for Injection, 75 mcg, 2 pack medication cartridges, Rx only, For subcutaneous use only, Manufactured for: Sh… by Shire Human Genetic Therapies, citing defective Delivery System: potential risk of rubber stopper particles clogging the needle and leading to underdosing.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0037-2020
ClassificationClass I
Statusterminated
Initiated2019-09-12
Published2019-10-02
Last updated2026-09-13 11:52 UTC
CompanyShire Human Genetic Therapies
DistributionUS

Product

Natpara (parathyroid hormone) for Injection, 75 mcg, 2 pack medication cartridges, Rx only, For subcutaneous use only, Manufactured for: Shire-NPS Pharmaceuticals, Inc., Lexington, MA NDC 68875-0204-02

Reason

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

Identifiers

code_info
06628462, exp 5/31/2020 06651000, exp 9/30/2020 06661659, exp 6/30/2020 07110125, 07301073, exp 10/31/2020 0720043…06628462, exp 5/31/2020 06651000, exp 9/30/2020 06661659, exp 6/30/2020 07110125, 07301073, exp 10/31/2020 07200435, 7/31/2020 07482211, exp 12/31/2020 07630714, exp 3/31/2021 NX170002DA, exp 12/31/2019 NX17004DA, exp 3/31/2020 NX17007DA, NX17007DB, NX17008DA exp 4/30/2020 NX17010DA, NX17012DA, exp 6/30/2020

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0037-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.