C. O. Truxton Recalls Doxycycline Hyclate Tablets Due to Wrong Bar Code
C. O. Truxton is recalling 287 bottles of Doxycycline Hyclate Tablets, 100 mg, because the product bears the wrong bar code.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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 minor labeling error (wrong bar code) with no reported illnesses or injuries, fitting the criteria for a moderate severity score.
Plain-English summary
C. O. Truxton is recalling 287 bottles of Doxycycline Hyclate Tablets, USP, 100 mg, 500-count bottles. The recall is due to a labeling error where the product bears the wrong bar code.
The affected product is distributed by Truxton Inc. in Bellmawr, NJ, and manufactured for Blu Caribe Dorado in Puerto Rico. The specific lot number is 13D0011FP8, with an expiration date of 09/15. The product is distributed nationwide.
Consumers should check their medication for the specific NDC numbers 0463-6000-50 or 24658-312-05 and the lot number 13D0011FP8. If the product matches these details, consumers should contact their pharmacist or healthcare provider for guidance on returning the product or obtaining a replacement.
The recalled product
- Product
- Doxycycline Hyclate Tablets, USP, 100 mg, 500-count bottle, Rx only, Distributed by: Truxton Inc. Bellmawr, NJ 08031, Manufactured for: Blu Caribe Dorado, PR 00646 USA, NDC 0463-6000-50 (top panel) NDC 24658-312-05 (side panel)
- Manufacturer
- C. O. Truxton
- Category
- Drug — Antibiotic
- Hazard
- Affected units
- 287
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 (2)
- Lot # 13D0011FP8
- Exp 09/15
Distribution
Distributed nationwide across the United States.
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