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Class II: temporary or reversible health riskTerminated

Pharm D Solutions Lipo MIC-12 Compound Injectable a) NDC Recall

Lipo MIC-12 Compound Injectable a) NDC 69699-1603-10

Pharm D Solutions, LLC · Houston, TX

Risk level
Class II
Reported by FDA
Nov 7, 2018
Recall ID
D-0166-2019
Check your lot numberHow we source this data

Summary

Pharm D Solutions recalled Lipo MIC-12 Compound Injectable a) NDC starting Sep 10, 2018. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0166-2019 on Nov 7, 2018. Reason: Lack of Assurance of Sterility. Status: Terminated.

Why it was recalled

Lack of Assurance of Sterility

Product description

Lipo MIC-12 Compound Injectable a) NDC 69699-1603-10; b) 30 mL Stock Solution Compound Injectable NDC 69699-1603-30, Pharm D Solutions, Houston, Texas

Lot numbers, UPCs & expiration codes

Lot: a) 09042018:66/A Discard by: 3/3/2019; 07302018:65 Discard by: 1/26/2019; b) 08132018:75/A Discard by: 2/1/2019; 04172018:16 Discard by: 9/30/2018; 03212018:27 Discard by: 9/17/2018; 04242018:82 Discard by: 10/20/2018; 05142018:72 Discard by: 11/10/2018; 06192018:67 Discard by: 12/18/2018; 08142018:00 Discard by: 2/1/2019; 07302018:64 Discard by: 1/26/2019

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-0166-2019
Classification
Class II
Status
Terminated
Recall initiated
Sep 10, 2018
FDA report date
Nov 7, 2018
Quantity
896 vials; 64000 milliliters
Recall type
Voluntary: Firm initiated
Recalling firm
Pharm D Solutions, LLC

Original FDA data

Every field from FDA enforcement report D-0166-2019, exactly as published.

Show all FDA fields
City
Houston
State
TX
Status
Terminated
Country
United States
Event ID
81002
Address
1304 S Loop W
Code information
Lot: a) 09042018:66/A Discard by: 3/3/2019; 07302018:65 Discard by: 1/26/2019; b) 08132018:75/A Discard by: 2/1/2019; 04172018:16 Discard by: 9/30/2018; 03212018:27 Discard by: 9/17/2018; 04242018:82 Discard by: 10/20/2018; 05142018:72 Discard by: 11/10/2018; 06192018:67 Discard by: 12/18/2018; 08142018:00 Discard by: 2/1/2019; 07302018:64 Discard by: 1/26/2019
Postal code
77054-4010
Report date
Nov 7, 2018
Product type
Drugs
Recall number
D-0166-2019
Classification
Class II
Recalling firm
Pharm D Solutions, LLC
Product quantity
896 vials; 64000 milliliters
Termination date
Feb 5, 2021
Reason for recall
Lack of Assurance of Sterility
Voluntary / mandated
Voluntary: Firm initiated
Product description
Lipo MIC-12 Compound Injectable a) NDC 69699-1603-10; b) 30 mL Stock Solution Compound Injectable NDC 69699-1603-30, Pharm D Solutions, Houston, Texas
Distribution pattern
Nationwide
Recall initiation date
Sep 10, 2018
Initial firm notification
Press Release
Center classification date
Nov 1, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0166-2019, published Nov 7, 2018. View the source record (openFDA) · FDA enforcement reports

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

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