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Class I: serious health riskTerminated

C. O. Truxton Phenobarbital Tablets Recall

Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-war…

C. O. Truxton · Bellmawr, NJ

Risk level
Class I
Reported by FDA
Aug 30, 2017
Recall ID
D-1111-2017
Check your lot numberHow we source this data

Summary

C. O. Truxton recalled Phenobarbital Tablets starting Apr 20, 2017. The FDA classified it as Class I (serious health risk) and published enforcement report D-1111-2017 on Aug 30, 2017. Reason: Labeling: Labeled Error on Declared Strength; report of a 1000 ct bottle labeled as Phenobarbital 15 mg tablets actually contained 30 mg tablets. Status: Terminated.

Why it was recalled

Labeling: Labeled Error on Declared Strength; report of a 1000 ct bottle labeled as Phenobarbital 15 mg tablets actually contained 30 mg tablets

Product description

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

Lot numbers, UPCs & expiration codes

Lot # 70952A; Exp. 11/17

Where it was sold

Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1111-2017
Classification
Class I
Status
Terminated
Recall initiated
Apr 20, 2017
FDA report date
Aug 30, 2017
Quantity
unknown
Recall type
Voluntary: Firm initiated
Recalling firm
C. O. Truxton

Original FDA data

Every field from FDA enforcement report D-1111-2017, exactly as published.

Show all FDA fields
City
Bellmawr
State
NJ
Status
Terminated
Country
United States
Event ID
77082
Address
136 Harding Ave
Code information
Lot # 70952A; Exp. 11/17
Postal code
08031-2412
Report date
Aug 30, 2017
Product type
Drugs
Recall number
D-1111-2017
Classification
Class I
Recalling firm
C. O. Truxton
Product quantity
unknown
Termination date
Sep 11, 2018
Reason for recall
Labeling: Labeled Error on Declared Strength; report of a 1000 ct bottle labeled as Phenobarbital 15 mg tablets actually contained 30 mg tablets
Voluntary / mandated
Voluntary: Firm initiated
Product description
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
Distribution pattern
Nationwide
Recall initiation date
Apr 20, 2017
Initial firm notification
Press Release
Center classification date
Aug 22, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1111-2017, published Aug 30, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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