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Class II: temporary or reversible health riskTerminated

FVS Holdings, Inc. dba. Green Valley Drugs Glycerin/Lidocaine/Epinephrine Injection Recall

Glycerin/Lidocaine/Epinephrine Injection including Glycerin 72% Lido:Epi 2-1-30 mL, Rx…

FVS Holdings, Inc. dba. Green Valley Drugs · Henderson, NV

Risk level
Class II
Reported by FDA
May 22, 2013
Recall ID
D-369-2013
Check your lot numberHow we source this data

Summary

FVS Holdings, Inc. dba. Green Valley Drugs recalled Glycerin/Lidocaine/Epinephrine Injection starting Apr 10, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-369-2013 on May 22, 2013. Reason: Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility assurance and concerns associated with the quality control processes. Status: Terminated.

Why it was recalled

Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility assurance and concerns associated with the quality control processes.

Product description

Glycerin/Lidocaine/Epinephrine Injection including Glycerin 72% Lido:Epi 2-1-30 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.

Lot numbers, UPCs & expiration codes

Lot #: 20130211-U, Exp 5/11/2013

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-369-2013
Classification
Class II
Status
Terminated
Recall initiated
Apr 10, 2013
FDA report date
May 22, 2013
Quantity
unknown
Recall type
Voluntary: Firm initiated
Recalling firm
FVS Holdings, Inc. dba. Green Valley Drugs

Original FDA data

Every field from FDA enforcement report D-369-2013, exactly as published.

Show all FDA fields
City
Henderson
State
NV
Status
Terminated
Country
United States
Event ID
64879
Address
1850 Whitney Mesa Dr
Address (line 2)
Suite 180
Code information
Lot #: 20130211-U, Exp 5/11/2013
Postal code
89014-2091
Report date
May 22, 2013
Product type
Drugs
Recall number
D-369-2013
Classification
Class II
Recalling firm
FVS Holdings, Inc. dba. Green Valley Drugs
Product quantity
unknown
Termination date
Mar 21, 2014
Reason for recall
Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility assurance and concerns associated with the quality control processes.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Glycerin/Lidocaine/Epinephrine Injection including Glycerin 72% Lido:Epi 2-1-30 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Distribution pattern
Nationwide
Recall initiation date
Apr 10, 2013
Initial firm notification
Press Release
Center classification date
May 16, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-369-2013, published May 22, 2013. View the source record (openFDA) · FDA enforcement reports

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

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