Bryant Ranch Prepack, Inc. recalls Morphine Sulfate extended-Release Tablets, USP; 60 mg, 100-count bottles, Rx only, manufactured by: Ohm Laboratories
Bryant Ranch Prepack recalls 60mg Morphine Sulfate extended-release tablets due to label mix-up. Some bottles contain 30mg instead of 60mg, which could lead to incorrect dosing.
Use caution until it’s fixed
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.
Contact the company & request your remedy
What happened, in plain English
Bryant Ranch Prepack is recalling 60 mg Morphine Sulfate extended-release tablets that may have incorrect labeling. This mix-up could lead to taking the wrong dose, which is dangerous for patients using these pain medications. Read more at govinfonow.com/recall/34614-bryant-ranch-prepack-morphine-sulfate-tablets-recall-label-mix-up.
Source Summary by GovInfoNow · govinfonow.com/recall/34614-bryant-ranch-prepack-morphine-sulfate-tablets-recall-label-mix-up · Updated September 23, 2026 · FDA enforcement record: FDA #D-1188-2022
Cite this page
“Bryant Ranch Prepack Morphine Sulfate Tablets Recall: Label Mix-Up Risk.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/34614-bryant-ranch-prepack-morphine-sulfate-tablets-recall-label-mix-up. Based on FDA recall #D-1188-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1188-2022%22&limit=1).
Why it’s dangerous
The tablets may have incorrect labeling, meaning some bottles contain 30 mg tablets labeled as 60 mg or 60 mg tablets labeled as 30 mg. This could cause patients to take a dose that is too high or too low, leading to serious health risks.
Who’s affected
Patients prescribed Morphine Sulfate extended-release tablets by a doctor are most at risk. This recall affects specific 60 mg tablets that may have been mislabeled as 30 mg or vice versa.
How to tell if you have this one
Check for bottles labeled 'Morphine Sulfate 60 mg Extended-Release' that contain 30 mg tablets or vice versa. The product was manufactured by Ohm Laboratories and sold by Bryant Ranch Prepack with NDC 63629-1089-01.
- Brand
Bryant Ranch Prepack- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
Distributed to one wholesaler in AL for further distribution in the US.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-1187-2022 | Morphine Sulfate extended-Release Tablets, USP; 30 mg, 100-count bottles, Rx only, manufactured by: Ohm Laboratories Inc., New Brunswick NJ 08901 USA; Relabeled by: Bryant Ranch Prepack, Inc., Burbank, CA, 91504 USA, NDC: 63629-1088-01.; Lot #: 179642, Exp. Date 11/30/2023. | — |
| D-1188-2022 | Morphine Sulfate extended-Release Tablets, USP; 60 mg, 100-count bottles, Rx only, manufactured by: Ohm Laboratories Inc., NJ; Relabeled by: Bryant Ranch Prepack, Inc, CA, NDC 63629-1089-01; Lot #: 179643, Exp. Date 08/31/2023. | — |
What to do — step by step
Check Label
Look for bottles labeled as Morphine Sulfate 60 mg Extended-Release that contain 30 mg tablets or vice versa.
Questions people ask
Why is this recall happening?
The recall is due to a label mix-up where some bottles contain the wrong strength of Morphine Sulfate tablets.
How do I know if I have the recalled product?
Check for bottles labeled 'Morphine Sulfate 60 mg Extended-Release' that contain 30 mg tablets or vice versa. The product was manufactured by Ohm Laboratories and sold by Bryant Ranch Prepack with NDC 63629-1089-01.
What should I do if I have the recalled product?
The recall does not specify a remedy, so check the label and contact your doctor or pharmacist for guidance.
Contact Bryant Ranch Prepack
We’ve drafted a message you can send Bryant Ranch Prepack to request your refund or repair — edit it as you like.
Subject: Recall D-1188-2022 — Bryant Ranch Prepack Bryant Ranch Prepack Hello, I own a Bryant Ranch Prepack that is covered by recall D-1188-2022 from Bryant Ranch Prepack. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1188-2022 (June 17, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1188-2022 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.