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Lower risk Drug recall · FDA · Published June 26, 2024

Dr. Reddy's Sevelamer Carbonate Packets Missing Lot/Exp Dates - Recall

Dr. Reddy's recalls Sevel: 0.8g oral suspension packets with missing lot and expiration dates. Consumers should check labels for correct dates to avoid potential safety issues.

🇺🇸 FDA recall #D-0625-2024DrugDr. Reddy's ›
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Recalling firmDr. Reddy's Laboratories, Inc.107 College Rd E · Princeton, NJ 08540-6623
✎ GovInfoNow plain-language explainer

Dr. Reddy's recalls Sevelamer Carbonate oral suspension packets that lack lot numbers and expiration dates. This labeling error could lead to confusion about product age and safety, especially for patients on long-term treatment. Read more at govinfonow.com/recall/32607-dr-reddy-s-sevelamer-carbonate-packets-missing-lot-exp-dates.

Source Summary by GovInfoNow · govinfonow.com/recall/32607-dr-reddy-s-sevelamer-carbonate-packets-missing-lot-exp-dates · Updated August 17, 2026 · FDA enforcement record: FDA #D-0625-2024

Cite this page

“Dr. Reddy's Sevelamer Carbonate Packets Missing Lot/Exp Dates - Recall.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/32607-dr-reddy-s-sevelamer-carbonate-packets-missing-lot-exp-dates. Based on FDA recall #D-0625-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0625-2024%22&limit=1).

The FDA announced on June 26, 2024, that Dr. Reddy's Laboratories, Inc. is recalling Sevelamer Carbonate for Oral Suspension 0.8g packets due to missing lot numbers and expiration dates on the packaging. The agency classified this as a Class III recall.

How to tell if you have it

  • Brand: Dr. Reddy's
  • Product: Sevelamer Carbonate for Oral Suspension 0.8g packets, packaged in 90 packets per container
  • Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540
  • NDC: 43598-478-90
  • Lot #: T2305999
  • Exp. Date: 11/2025
  • Quantity: 5,136 cartons
  • Distribution: Nationwide within the United States

The hazard

The recall addresses labeling issues involving incorrect or missing lot numbers and expiration dates on the packets. The FDA stated that the missing lot number and expiration dates were found on the product.

Context

GovInfoNow's records show Dr. Reddy's Laboratories, Inc. has 85 other recalls on record since April 9, 2012. Other recent recalls of similar products include Dr. Reddy's Varenicline Tablets Recall (November 11, 2025), Dr. Reddy's Succinylcholine Chloride Injection Recall (September 26, 2025), and Dr. Reddy's Omeprazole Capsules Recall (June 30, 2025). Other recent recalls of similar products include Sandoz Focalin XR 5mg Capsules: Missing Lot/Exp Date Recall (June 1, 2026), Haleon Parodontax Mouthwash Recall: Missing Lot/Exp Date on 500mL Bottles (December 26, 2025), and Kirkman Lidocaine Cream Recall: Stability Issues May Affect Expiry Date (February 18, 2026).

How to tell if you have this one

Check for packets labeled with lot number T2305999 and expiration date 11/2025. The product is packaged in 90 packets per container and distributed by Dr. Reddy's Laboratories Inc.

  • Brand
    Dr. Reddy's
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Labels

    Look for the lot number T2305999 and expiration date 11/2025 on the packets.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide within the United States” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 49 days after the firm started it.

1. Firm started the recall: Jun 26, 202412. FDA classified it Class III: Aug 2, 202423. Published in FDA’s Enforcement Report: Aug 14, 202432024
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

What should I do if I have the recalled product?

The recall does not require immediate action, but you should check the labels for the correct lot and expiration dates to ensure safe use.

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Where this comes from

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-0625-2024 (June 26, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0625-2024 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA