RecallRadar

FDA Drug recall D-0006-2017

Vyvanse (lisdexamfetamine dimesylate) Capsules 30 mg, 100 count bottle, Rx Only, Manufactured for: Shire US, Inc., Lexington, MA 02421, NDC…

On 2016-10-12 the FDA classified a Class III recall of Vyvanse (lisdexamfetamine dimesylate) Capsules 30 mg, 100 count bottle, Rx Only, Manufactured for: Shire US, Inc., Lexington, MA 02421, NDC… by Shire, citing presence of Foreign Tablets/Capsules.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0006-2017
ClassificationClass III
Statusterminated
Initiated2016-09-02
Published2016-10-12
Last updated2026-09-13 11:51 UTC
CompanyShire
DistributionUS

Product

Vyvanse (lisdexamfetamine dimesylate) Capsules 30 mg, 100 count bottle, Rx Only, Manufactured for: Shire US, Inc., Lexington, MA 02421, NDC 59417-103-10

Reason

Presence of Foreign Tablets/Capsules

Identifiers

ndc59417-101-10
ndc59417-102-10
ndc59417-103-10
ndc59417-104-10
ndc59417-105-10
ndc59417-106-10
ndc59417-107-10
ndc59417-115-01
ndc59417-116-01
ndc59417-117-01
ndc59417-118-01
ndc59417-119-01
ndc59417-120-01
code_infoLot # AF3360B; Exp. 04/19

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0006-2017%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.