RecallRadar

FDA Drug recall D-0036-2020

Natpara (parathyroid hormone) for Injection, 50 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, 50 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-0036-2020
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, 50 mcg, 2 pack medication cartridges, Rx only, For subcutaneous use only, Manufactured for: Shire-NPS Pharmaceuticals, Inc., Lexington, MA NDC 68875-0203-02

Reason

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

Identifiers

code_info
06628461, exp 8/31/2020 06661658, 07110136, 7164106, 07761970 exp 10/31/2020 07630717, 08689119, exp 12/31/2020 0776…06628461, exp 8/31/2020 06661658, 07110136, 7164106, 07761970 exp 10/31/2020 07630717, 08689119, exp 12/31/2020 07769458, exp 4/30/2021 07983643, 08003758, exp 6/30/2021 08214790, exp 8/31/2020 NY17002DA, NY17002DB, 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-0036-2020%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.