CLASS III Drug recall · Reported 13 Feb 2013 · FDA Enforcement Report
Methocarbamol 750 mg Tablets, 90-count bottle, Mfg by: West-Ward recalled
Stat Rx U is recalling Methocarbamol 750 mg Tablets, 90-count bottle, Mfg by: West-Ward, distributed in Pennsylvania. The recall was initiated on 28 Jan 2013 and the FDA has classified it as Class III.
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-144-2013
- FDA event ID
- 64223
- Recalling firm
- Stat Rx U, Gainesville, GA
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 28 Jan 2013
- FDA classified
- 4 Feb 2013
- Reported
- 13 Feb 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Packaging Defects
Timeline
| 28 Jan 2013 | Recall initiated by company | |
| 4 Feb 2013 | Classified by FDA | +7 days |
| 13 Feb 2013 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Labeling: Incorrect or missing lot and/or expiration date. The product was mistakenly labeled with an expiration date of 10/16 instead of 01/16.
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 750 mg Tablets, 90-count bottle, Mfg by: West-Ward Pharm. Corp., Eatontown, NJ 07724, Packaged and Distributed by: Stat Rx USA, NDC 42549-521-90.
Where it was distributed
PA
Questions about this recall
Is Methocarbamol 750 mg Tablets, 90-count bottle, Mfg by: West-Ward recalled?
Yes. Stat Rx U recalled Methocarbamol 750 mg Tablets, 90-count bottle, Mfg by: West-Ward on 28 Jan 2013. The recall is Class III and its status is Terminated. Recall number D-144-2013.
Why was it recalled?
Labeling: Incorrect or missing lot and/or expiration date. The product was mistakenly labeled with an expiration date of 10/16 instead of 01/16.
Which lots are affected?
A02568, Exp 01/16
Where was it sold?
PA
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 III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 21 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 Stat Rx U
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|---|---|---|---|---|---|
| Drug | CLASS III | Venlafaxine ER 150mg, 30 Tabs, Generic for: Effexor, Packaged recalled | Stat Rx U | Labeling Errors | GA, TN |
| Drug | CLASS III | Tobramycin Ophthalmic Oint., 3%, (Generic for: Tobrex) recalled | Stat Rx U | Sterility | FL, PA, VA |
| Drug | CLASS III | Tizanidine (Generic for: Zanaflex), 4 mg recalled by Stat Rx U | Stat Rx U | Packaging Defects | Nationwide |