Succinylcholine Chloride Recall: Dr. Reddy's (Lot K250048)
The recall concerns Succinylcholine Chloride Injection, USP, 200 mg/10 mL, 25 x 10 mL vials, Rx Only, distributed nationwide in the USA. The trigger was an out-of-specification result during the 6-month stability testing with decreased preservative concentration. A total of 571 vials are involved in this recall, identified by Lot # K250048.
| Brand | Dr. Reddy's Laboratories, Inc. |
|---|---|
| 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. |
| Severity | moderate |
| Units affected | 4800 |
| Distribution | Nationwide within the USA. |
| Agency | FDA |
WHAT YOU SHOULD DO
- Do not use any affected vials and verify your lot number (K250048) against your product.
- Contact your healthcare provider or pharmacist for guidance on replacement or returns.
- If you have the affected vials, follow disposal or return instructions provided by your supplier or local regulations.
How to identify the recalled item
| Lot / date codes | Lot # K250048 |
|---|---|
| Lot / date codes | Lot # F2400244, Exp Date: 10/31/2026 |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.