CLASS I Drug recall · Reported 10 Nov 2021 · FDA Enforcement Report
Methocarbamol 500mg Tablet recalled by Bryant Ranch Prepack
Bryant Ranch Prepack is recalling Methocarbamol 500mg Tablet, distributed nationwide in the US. The recall was initiated on 12 Oct 2021 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0092-2022
- FDA event ID
- 88861
- Recalling firm
- Bryant Ranch Prepack, Burbank, CA
- Classification
- Class I
- Status
- Completed
- Recall initiated
- 12 Oct 2021
- FDA classified
- 2 Nov 2021
- Reported
- 10 Nov 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Packaging Defects
Timeline
| 12 Oct 2021 | Recall initiated by company | |
| 2 Nov 2021 | Classified by FDA | +21 days |
| 10 Nov 2021 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504
Where it was distributed
Nationwide in the US
Questions about this recall
Why was it recalled?
Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets
Which lots are affected?
Lot #: 163935, Exp: 10/31/2022
Where was it sold?
Nationwide in the US
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Bryant Ranch Prepack
All 17| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Cephalexin for Oral Suspension, USP, 125mg recalledCephalexin | Bryant Ranch Prepack | Other | Nationwide |
| Drug | CLASS III | Cephalexin for Oral Suspension, USP, 250mg recalledCephalexin | Bryant Ranch Prepack | Other | Nationwide |
| Drug | CLASS III | Cephalexin for Oral Suspension, USP, 250mg recalledCephalexin | Bryant Ranch Prepack | Other | Nationwide |
| Drug | CLASS III | Cephalexin for Oral Suspension, USP, 250mg recalledCephalexin | Bryant Ranch Prepack | Other | Nationwide |
| Drug | CLASS III | Cephalexin for Oral Suspension, USP, 125mg recalledCephalexin | Bryant Ranch Prepack | Other | Nationwide |
Other Methocarbamol recalls
All 7| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Methocarbamol Injection USP 1,000 mg/ (100 mg/mL) Single Dose Vial recalledMethocarbamol | Somerset Therapeutics Private | Sterility | Nationwide |
| Drug | CLASS I | Methocarbamol Injection, USP 1000mg recalled by Eugia USMethocarbamol | Eugia US | Particulate Matter | Nationwide |
| Drug | CLASS II | Methocarbamol recalled by American Pharmaceutical | American Pharmaceutical Ingredients | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | Methocarbamol Tablets, USP 500 mg recalled | Golden State Medical Supply | Packaging Defects | GA |
| Drug | CLASS II | Methocarbamol, Tablet, 500 mg recalled by Aidapak Services | Aidapak Services | Labeling Errors | 4 states |