Desmopressin Acetate Tablet recall: Subpotent
Desmopressin Acetate Tablet, 0.2 mg, 100-count box, Rx only, Source NDC: 23155-0490-01; MFG: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816…
Why was Desmopressin Acetate Tablet recalled?
Subpotent Drug: repackaged product was recalled by the manufacturer for subpotency.
What should I do if I have this product?
Review the official FDA enforcement record for current 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 # B1817019-082222, Exp. 02/24/2023; B1819127-082322, Exp. 02/26/2023
- Product
- Desmopressin Acetate Tablet, 0.2 mg, 100-count box, Rx only, Source NDC: 23155-0490-01; MFG: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816…
- Recalling firm
- RemedyRepack Inc.
- Quantity
- 9 boxes
- Distribution
- Product was distributed to two different customers in MI.
- Recall date
- December 14, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)