RecallRadar

FDA Drug recall D-0008-2026

Succinylcholine Chloride Injection, USP, 200 mg/10 mL (20 mg/mL), 25 x 10 mL Multiple-Dose Vials, For Intravenous or Intramuscular use, Rx…

On 2025-10-15 the FDA classified a Class II recall of Succinylcholine Chloride Injection, USP, 200 mg/10 mL (20 mg/mL), 25 x 10 mL Multiple-Dose Vials, For Intravenous or Intramuscular use, Rx… by Dr Reddy S Laboratories, citing out-of-Specification (OOS) result during the 6-month stability testing; decreased preservative concentration.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0008-2026
ClassificationClass II
Statusongoing
Initiated2025-09-26
Published2025-10-15
Last updated2026-09-13 11:52 UTC
CompanyDr Reddy S Laboratories
DistributionUS

Product

Succinylcholine Chloride Injection, USP, 200 mg/10 mL (20 mg/mL), 25 x 10 mL Multiple-Dose Vials, For Intravenous or Intramuscular use, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540. NDC: 43598-666-25

Reason

Out-of-Specification (OOS) result during the 6-month stability testing; decreased preservative concentration.

Identifiers

ndc43598-666-11
ndc43598-666-25
code_infoLot # K250048

Status history

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

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0008-2026%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.