RecallRadar

FDA Drug recall D-0180-2023

Epinephrine (L-Adrenaline), USP, CAS 51-43-4, Packaged in amber glass bottles in a vacuum sealed pouch as (a)100 G

On 2023-02-01 the FDA classified a Class I recall of Epinephrine (L-Adrenaline), USP, CAS 51-43-4, Packaged in amber glass bottles in a vacuum sealed pouch as (a)100 G by Spectrum Laboratory Products, citing discoloration: Product complaints of the repackaged Epinephrine API being discolored which could result in less effective product.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0180-2023
ClassificationClass I
Statusterminated
Initiated2022-12-19
Published2023-02-01
Last updated2026-09-13 11:52 UTC
CompanySpectrum Laboratory Products
DistributionUS

Product

Epinephrine (L-Adrenaline), USP, CAS 51-43-4, Packaged in amber glass bottles in a vacuum sealed pouch as (a)100 G; (b)1 G, (c) 25 G, (d) 5 G; Rx only. Repackaged by Spectrum Chemical Mfg. Corp. Gardena, CA 90248; New Brunswick, NJ 08901.

Reason

Discoloration: Product complaints of the repackaged Epinephrine API being discolored which could result in less effective product

Identifiers

code_infoLot # (a) (b) (c) (d) lot 2KL0353, EXP 30-Sep-2023; 2KF0151, EXP 31-Mar-2023

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-0180-2023%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.