Lower riskDrug recall · FDA · Published September 26, 2025
Dr. Reddy's Succinylcholine Chloride Injection Recall: Stability Testing Issue
Dr. Reddy's recalls 25 vials of Succinylcholine Chloride Injection due to decreased preservative concentration found during stability testing. This may affect medication safety.
“Dr. Reddy's Succinylcholine Chloride Injection Recall: Stability Testing Issue.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/31768-dr-reddy-s-succinylcholine-chloride-injection-recall-stability-testing-issue. Based on FDA recall #D-0008-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0008-2026%22&limit=1).
The Food and Drug Administration announced on Sept. 26, 2025, that Dr. Reddy's Laboratories Inc. voluntarily recalled Succinylcholine Chloride Injection due to out-of-specification stability testing results indicating decreased preservative concentration.
How to tell if you have it
Brand: Dr. Reddy's
Product: Succinylcholine Chloride Injection, USP, 200 mg/10 mL (20 mg/mL), 25 x 10 mL Multiple-Dose Vials
NDC: 43598-666-25
Lot #: K250048
The hazard
The recall addresses out-of-specification results during six-month stability testing that revealed a decreased preservative concentration in the drug product.
Context
GovInfoNow's records show Dr. Reddy's Laboratories, Inc. has 85 other recalls on record since April 9, 2012. Recent brand recalls include a Nov. 11, 2025, Varenicline Tablets recall for subpotent drug risk and a June 30, 2025, Omeprazole Capsules recall for foreign tablets found. Other recent recalls of similar products include Blaine Labs TERPENICOL Antifungal Solution Recall (April 8, 2026), Somerset Therapeutics Cisatracurium Besylate Injection Recall (Nov. 26, 2025), and Safecor Health Fluphenazine Elixir Recall (Aug. 13, 2026).
How to tell if you have this one
Look for vials labeled 'Succinylcholine Chloride Injection, USP, 200 mg/10 mL (20 mg/mL), 25 x 10 mL Multiple-Dose Vials' with NDC code 43598-666-25 and lot number K250048.
Brand
Dr. Reddy's
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Product Details
Verify the product label includes NDC 43598-666-25 and lot number K250048.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Nationwide within the USA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 19 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #D-0008-2026 (September 26, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0008-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.