FDA recall record

Sevelamer Carbonate for Oral Suspension 0.8g packets recall — FDA D-0625-2024

Labeling: Incorrect or Missing Lot and/or Exp Date. Missing lot number and expiration dates on packets

Class IIIclassification
D-0625-2024official record ID
Aug 14, 2024report date

Recall record at a glance

Official recordD-0625-2024
CategoryDrug Recalls
ClassificationClass III
FDA record statusOngoing
Recalling firmDr. Reddy's Laboratories, Inc.
Report dateAug 14, 2024
Recall initiation dateJun 26, 2024
Quantity5,136 cartons
LocationPrinceton, NJ, United States

Official product description

Sevelamer Carbonate for Oral Suspension 0.8g packets, packaged in 90 packets per container, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India NDC 43598-478-90

Why the product was recalled

Labeling: Incorrect or Missing Lot and/or Exp Date. Missing lot number and expiration dates on packets

Distribution information

Nationwide within the United States

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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