RecallRadar

FDA Drug recall D-0038-2020

Natpara (parathyroid hormone) for Injection, 100 mcg, 2 pack medication cartridges, Rx only, For subcutaneous use only, Manufactured for: S…

On 2019-10-02 the FDA classified a Class I recall of Natpara (parathyroid hormone) for Injection, 100 mcg, 2 pack medication cartridges, Rx only, For subcutaneous use only, Manufactured for: S… 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-0038-2020
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, 100 mcg, 2 pack medication cartridges, Rx only, For subcutaneous use only, Manufactured for: Shire-NPS Pharmaceuticals, Inc., Lexington, MA 68875-0205-02

Reason

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

Identifiers

code_info
06828752, exp 12/31/2019 07110118, exp 4/30/2021 07164107, exp 12/31/2019 07200436, 07301074, exp 4/30/2021 074…06828752, exp 12/31/2019 07110118, exp 4/30/2021 07164107, exp 12/31/2019 07200436, 07301074, exp 4/30/2021 07482212, 07630715, exp 6/30/2021 07769460, exp 4/30/2021

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-0038-2020%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.