Gelatin Capsule Pack for use with the Sodium Iodide recall
Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing 5 empty capsules and 5 Dibasic Sodium Phosphate Capsules 300 mg…
Why was Gelatin Capsule Pack for use with the Sodium Iodide recalled?
Failed Tablet/Capsule Specifications
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot, expiry: Lot 3666245, exp: 02/28/2026; Lot 4546213, exp: 02/28/2026 and Lot 4951280, exp 09/30/2027
- Product
- Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing 5 empty capsules and 5 Dibasic Sodium Phosphate Capsules 300 mg…
- Recalling firm
- Radnostix
- Quantity
- 2,699 blister cartons
- Distribution
- Nationwide in the US, including Puerto Rico
- Recall date
- April 1, 2026
- Classification
- Class III
- Status
- Ongoing
- Agency
- FDA (drug)