Morphine Sulfate extended-Release Tablets recall: Labeling Error
Morphine Sulfate extended-Release Tablets, USP; 60 mg, 100-count bottles, Rx only, manufactured by: Ohm Laboratories Inc., NJ; Relabeled by: Bryant…
Why was Morphine Sulfate extended-Release Tablets recalled?
Labeling: Label Mix-up: bottles labeled as Morphine Sulfate 60 mg Extended-Release tablets contain Morphine Sulfate 30 mg Extended-Release tablets and bottles labeled as Morphine Sulfate 30 mg Extended-Release tablets may contain Morphine Sulfate 60 mg Extended-Release tablets.
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 #: 179643, Exp. Date 08/31/2023.
- Product
- Morphine Sulfate extended-Release Tablets, USP; 60 mg, 100-count bottles, Rx only, manufactured by: Ohm Laboratories Inc., NJ; Relabeled by: Bryant…
- Recalling firm
- Bryant Ranch Prepack, Inc.
- Distribution
- Distributed to one wholesaler in AL for further distribution in the US.
- Recall date
- July 20, 2022
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)