Sevelamer Carbonate for Oral Suspension missing lot and expiration date labels
Dr. Reddy's Laboratories is recalling Sevelamer Carbonate for Oral Suspension packets missing lot number and expiration date information. Approximately 5,136 cartons were distributed nationwide.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: FDA Class III recall for missing lot number and expiration date information on packets. This is a documentation and labeling issue with no reported safety hazard, product defect, or illnesses or injuries.
Plain-English summary
Dr. Reddy's Laboratories, Inc. is recalling Sevelamer Carbonate for Oral Suspension in 0.8g packets due to missing lot number and expiration date information on the packet labels.
The affected lot is T2305999, which has an expiration date of November 2025. Approximately 5,136 cartons were distributed nationwide within the United States.
The packets lack printed lot numbers and expiration dates, which are required labeling elements for pharmaceutical products. This recall is classified by the FDA as Class III.
The recalled product
- Product
- SEVELAMER CARBONATE FOR ORAL SUSPENSION (SEVELAMER CARBONATE FOR ORAL SUSPENSION)
- Brand
- SEVELAMER CARBONATE FOR ORAL SUSPENSION
- Manufacturer
- Dr. Reddy's Laboratories, Inc.
- Category
- Drug
- Affected units
- 5,136
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Lot #: T2305999
- Exp. Date 11/2025
Distribution
Distributed nationwide across the United States.
Related recalls
Same manufacturer · Dr. Reddy's Laboratories, Inc.
See all →- ModerateVarenicline tablets recalled after an assay value fell below specification
FDA (Drugs) · 2025-12-17
- Moderate
- HighOmeprazole capsule bottle contained a foreign divalproex sodium tablet
FDA (Drugs) · 2025-07-23
- SevereLevetiracetam Injection Label Mismatch Nationwide Recall
FDA (Drugs) · 2025-04-23
- ModerateFDA Recalls JAVYGTOR Tablets Due to Failed Impurities and Degradation Specifications
FDA (Drugs) · 2024-12-18
Same hazard · missing lot number
See all →- LowFocalin XR 5mg capsules carry incorrect or missing lot and expiry
FDA (Drugs) · 2026-06-24
- ModerateMedline Endo Kit Recall: Missing Lot and Expiration Date Labels
FDA (Devices) · 2024-12-04