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Class II: temporary or reversible health riskTerminated

Kalman Health & Wellness, Inc. dba Essential Wellness Pharma Hcg 1000 U/ Lido 0 Recall

HCG 1000 U/ LIDO 0

Kalman Health & Wellness, Inc. dba Essential Wellness Pharma · Peoria, IL

Risk level
Class II
Reported by FDA
Nov 25, 2015
Recall ID
D-307-2016
Check your lot numberHow we source this data

Summary

Kalman Health & Wellness, Inc. dba Essential Wellness Pharma recalled Hcg 1000 U/ Lido 0 starting Sep 3, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-307-2016 on Nov 25, 2015. Reason: Lack of Assurance of Sterility: A recall of all compounded sterile preparations within expiry is being initiated due to observations associated with poor sterile production practices resulting in a lack of sterility assurance for their finished drugs. Status: Terminated.

Why it was recalled

Lack of Assurance of Sterility: A recall of all compounded sterile preparations within expiry is being initiated due to observations associated with poor sterile production practices resulting in a lack of sterility assurance for their finished drugs.

Product description

HCG 1000 U/ LIDO 0.2%/mL Injection, packaged in a) 3 mL and b) 8 mL vials, Rx only, Essential Wellness PHARMACY, 4625 N. University, Peoria, IL 61614.

Lot numbers, UPCs & expiration codes

Lot #: 080415, Exp 09/04/2015; and 4721-081715, Exp 09/17/2015

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-307-2016
Classification
Class II
Status
Terminated
Recall initiated
Sep 3, 2015
FDA report date
Nov 25, 2015
Quantity
2 vials
Recall type
Voluntary: Firm initiated
Recalling firm
Kalman Health & Wellness, Inc. dba Essential Wellness Pharma

Original FDA data

Every field from FDA enforcement report D-307-2016, exactly as published.

Show all FDA fields
City
Peoria
State
IL
Status
Terminated
Country
United States
Event ID
72241
Address
4625 N University St
Code information
Lot #: 080415, Exp 09/04/2015; and 4721-081715, Exp 09/17/2015
Postal code
61614-5828
Report date
Nov 25, 2015
Product type
Drugs
Recall number
D-307-2016
Classification
Class II
Recalling firm
Kalman Health & Wellness, Inc. dba Essential Wellness Pharma
Product quantity
2 vials
Termination date
Dec 29, 2017
Reason for recall
Lack of Assurance of Sterility: A recall of all compounded sterile preparations within expiry is being initiated due to observations associated with poor sterile production practices resulting in a lack of sterility assurance for their finished drugs.
Voluntary / mandated
Voluntary: Firm initiated
Product description
HCG 1000 U/ LIDO 0.2%/mL Injection, packaged in a) 3 mL and b) 8 mL vials, Rx only, Essential Wellness PHARMACY, 4625 N. University, Peoria, IL 61614.
Distribution pattern
Nationwide
Recall initiation date
Sep 3, 2015
Initial firm notification
Letter
Center classification date
Nov 17, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-307-2016, published Nov 25, 2015. 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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