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Class II: temporary or reversible health riskTerminated

VistaPharm Methadone Hydrochloride Oral Concentrate Recall

Methadone Hydrochloride Oral Concentrate, USP 10 mg/mL C-II, a

VistaPharm, Inc. · Largo, FL

Risk level
Class II
Reported by FDA
Feb 8, 2017
Recall ID
D-0465-2017
Check your lot numberHow we source this data

Summary

VistaPharm recalled Methadone Hydrochloride Oral Concentrate starting Jan 18, 2017. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0465-2017 on Feb 8, 2017. Reason: CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia. Status: Terminated.

Why it was recalled

CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.

Product description

Methadone Hydrochloride Oral Concentrate, USP 10 mg/mL C-II, a.) 1 fl. oz. (30 mL), 12 bottles per case (NDC No. 66689-695-30), b). 1 liter (1000 mL), 4 bottles per case, (NDC No. 66689-695-79), Rx only, Manufactured by VistaPharm, Largo, FL 33771.

Lot numbers, UPCs & expiration codes

a). Lot No. 416600 (Exp. 09/17) b). Lot No.449100 , 447500 (Exp. 04/18), 421800 (Exp. 10/17), 418600 (Exp. 09/17), 408700 (Exp. 06/17), 411900 (Exp. 07/17), 413800 (Exp. 08/17), 416500 (Exp. 09/17), 408500 (Exp. 06/17), 389800 (Exp. 01/17), 429900 (Exp. 12/17), 406300, 406100 (Exp. 05/17), 429700 (Exp. 12/17), 427300, 427100, 425900 (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-0465-2017
Classification
Class II
Status
Terminated
Recall initiated
Jan 18, 2017
FDA report date
Feb 8, 2017
Quantity
127,193 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
VistaPharm, Inc.

Original FDA data

Every field from FDA enforcement report D-0465-2017, exactly as published.

Show all FDA fields
City
Largo
State
FL
Status
Terminated
Country
United States
Event ID
75650
Address
7265 Ulmerton Rd
Code information
a). Lot No. 416600 (Exp. 09/17) b). Lot No.449100 , 447500 (Exp. 04/18), 421800 (Exp. 10/17), 418600 (Exp. 09/17), 408700 (Exp. 06/17), 411900 (Exp. 07/17), 413800 (Exp. 08/17), 416500 (Exp. 09/17), 408500 (Exp. 06/17), 389800 (Exp. 01/17), 429900 (Exp. 12/17), 406300, 406100 (Exp. 05/17), 429700 (Exp. 12/17), 427300, 427100, 425900 (11/17)
Postal code
33771-4809
Report date
Feb 8, 2017
Product type
Drugs
Recall number
D-0465-2017
Classification
Class II
Recalling firm
VistaPharm, Inc.
Product quantity
127,193 bottles
Termination date
Aug 26, 2021
Reason for recall
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Methadone Hydrochloride Oral Concentrate, USP 10 mg/mL C-II, a.) 1 fl. oz. (30 mL), 12 bottles per case (NDC No. 66689-695-30), b). 1 liter (1000 mL), 4 bottles per case, (NDC No. 66689-695-79), Rx only, Manufactured by VistaPharm, Largo, FL 33771.
Distribution pattern
Nationwide
Recall initiation date
Jan 18, 2017
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Feb 2, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0465-2017, published Feb 8, 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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