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Class II · ModerateActive recall

Succinylcholine

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot # K250048
Where it was soldNationwide within the USA.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

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

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byDr.Reddy's Laboratories Inc.,
Brand nameSUCCINYLCHOLINE
Generic nameSUCCINYLCHOLINE
Active ingredient(s)SUCCINYLCHOLINE CHLORIDE
Distributed by / forDr. Reddy's Laboratories, Inc.
NDC43598-666-25
Show the full FDA record
Full product labelSuccinylcholine 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
Recalling firmDr. Reddy's Laboratories, Inc.
DistributionNationwide within the USA.
Quantity571 vials
Recall initiated2025-09-26
Report date2025-10-15
Recall completed—
Recall numberD-0008-2026
ClassificationClass II
FDA statusOngoing
Origin on filePrinceton NJ United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.