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Class I: serious health riskTerminated

Avkare TraZODONE Hydrochloride Tablets 100 mg Recall

TraZODONE Hydrochloride Tablets USP 100 mg, Rx Only, 1000-count Bottle, Manufactured fo…

AVKARE Inc. · Pulaski, TN

Risk level
Class I
Reported by FDA
Dec 23, 2020
Recall ID
D-0168-2021
Check your lot numberHow we source this data

Summary

Avkare recalled TraZODONE Hydrochloride Tablets 100 mg starting Dec 7, 2020. The FDA classified it as Class I (serious health risk) and published enforcement report D-0168-2021 on Dec 23, 2020. Reason: Product mix-up: Bottles of sildenafil and trazodone were inadvertently packaged together during bottling at a 3rd party facility. Status: Terminated.

Why it was recalled

Product mix-up: Bottles of sildenafil and trazodone were inadvertently packaged together during bottling at a 3rd party facility.

Product description

TraZODONE Hydrochloride Tablets USP 100 mg, Rx Only, 1000-count Bottle, Manufactured for: AvKARE Pulaski, TN 38478, NDC 42291-834-10

Lot numbers, UPCs & expiration codes

Lot: 36783 Exp. 06/2022

Where it was sold

Nationwide within the U.S.

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-0168-2021
Classification
Class I
Status
Terminated
Recall initiated
Dec 7, 2020
FDA report date
Dec 23, 2020
Quantity
14368 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
AVKARE Inc.

Original FDA data

Every field from FDA enforcement report D-0168-2021, exactly as published.

Show all FDA fields
City
Pulaski
State
TN
Status
Terminated
Country
United States
Event ID
86940
Address
615 N 1st St
Code information
Lot: 36783 Exp. 06/2022
Postal code
38478-2403
Report date
Dec 23, 2020
Product type
Drugs
Recall number
D-0168-2021
Classification
Class I
Recalling firm
AVKARE Inc.
Product quantity
14368 bottles
Termination date
Oct 16, 2023
Reason for recall
Product mix-up: Bottles of sildenafil and trazodone were inadvertently packaged together during bottling at a 3rd party facility.
Voluntary / mandated
Voluntary: Firm initiated
Product description
TraZODONE Hydrochloride Tablets USP 100 mg, Rx Only, 1000-count Bottle, Manufactured for: AvKARE Pulaski, TN 38478, NDC 42291-834-10
Distribution pattern
Nationwide within the U.S.
Recall initiation date
Dec 7, 2020
Initial firm notification
Letter
Center classification date
Dec 16, 2020

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0168-2021, published Dec 23, 2020. 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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