Drug recall

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

FDA recall event 97690 · Class II · Dr. Reddy's Laboratories, Inc.

Key facts

Event ID 97690
Recall numbers D-0008-2026
Recalling firm Dr. Reddy's Laboratories, Inc.
Product type Drugs
Products 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…
Classification Class II
Status Ongoing
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Out-of-Specification (OOS) result during the 6-month stability testing; decreased preservative concentration.
Initiation date Sep 26, 2025
Report date Oct 15, 2025
City Princeton
State NJ
Country United States
FEI number 3011009040

At a glance

  • 1–9 Products in this recall
  • 1–9 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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