FDA Drug Recalls

Recalls / Class II

Class IID-306-2016

Product

HCG 1000 Units/mL SUB-Q Injection, packaged in a)1.5 mL, b) 2 mL, c) 2.4 mL, d) 4 mL, e) 6 mL, f) 7.5 mL, g) 8 mL, and h) 9 mL vials, Rx only, Essential Wellness PHARMACY, 4625 N. University, Peoria, IL 61614.

Affected lot / code info
Lot #: 080415, Exp 09/04/2015; 080515, Exp 09/05/2015; 080615, Exp 09/06/2015; 080715, Exp 09/07/2015; 081015, Exp 09/10/2015; 081115, Exp 09/11/2015; 081215, Exp 09/12/2015; 081315, Exp 09/13/2015; 081415, Exp 09/14/2015; 1702-081715, Exp 09/17/2015; 1702-081815, Exp 09/18/2015; and 1702-081915, Exp 09/19/2015

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.

Recalling firm

Firm
Kalman Health & Wellness, Inc. dba Essential Wellness Pharma
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
4625 N University St, N/A, Peoria, Illinois 61614-5828

Distribution

Quantity
49 vials
Distribution pattern
Nationwide

Timeline

Recall initiated
2015-09-03
FDA classified
2015-11-17
Posted by FDA
2015-11-25
Terminated
2017-12-29
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-306-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls