C. O. Truxton Recalls Phenobarbital Tablets Due to Labeling Error
C. O. Truxton is recalling specific lots of Phenobarbital Tablets USP, 15 mg, due to a label mixup that may result in mislabeled products.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II and involves a labeling error (label mixup) without reported injuries or illnesses, fitting the criteria for moderate severity involving minor labeling errors or low-risk contamination.
Plain-English summary
C. O. Truxton is voluntarily recalling specific lots of Phenobarbital Tablets USP, 15 mg, 1000 count bottles. The recall was initiated because of a labeling error described as a label mixup, which means the products may be mislabeled.
The affected products are manufactured by West-ward Pharmaceutical Corp. and distributed by Truxton, Inc. The recall covers three specific lots: Lot # 71162A (Exp. 10/18), Lot # 70915A (Exp. 08/17), and Lot # H15A55 (Exp. 11/17). The products were distributed nationwide.
Consumers and healthcare providers should check their inventory for these specific lot numbers and expiration dates. If found, the products should be returned to the distributor or disposed of according to local regulations. Patients should consult their healthcare provider for alternative medication if necessary.
The recalled product
- Product
- Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6160-10
- Manufacturer
- C. O. Truxton
- Category
- Drug — Prescription Medication
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- Lot # 71162A
- Exp. 10/18 Lot # 70915A
- Exp. 08/17 Lot # H15A55
- Exp. 11/17
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 6 recalled by C. O. Truxton under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 6 products in this recall →Related recalls
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