The Recall Desk
Agency classClass IIOur severity:SevereFDA (Drugs)·D-308-2016·Announced 2015-11-25

FDA Recalls HCG Injection Vials Due to Sterility Concerns

FDA is recalling HCG 2000 Units/mL Injection vials from Essential Wellness Pharmacy due to poor sterile production practices.

The agency’s classification

FDA (Drugs): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The agency classified this as an FDA Class II recall. Per the rubric, FDA Class II recalls involving significant risks such as lack of sterility assurance in injectable drugs are categorized as Severe.

Plain-English summary

The U.S. Food and Drug Administration (FDA) is recalling HCG 2000 Units/mL Injection, packaged in 4 mL and 15 mL vials. The product is prescription-only and was distributed nationwide by Kalman Health & Wellness, Inc. dba Essential Wellness Pharma, located in Peoria, Illinois.

The recall was initiated because of observations associated with poor sterile production practices. These practices resulted in a lack of assurance of sterility for the finished drugs. The affected lots are 080415 (expiration 09/04/2015) and 080715 (expiration 09/07/2015).

Consumers who have these products should stop using them and contact their healthcare provider or the recalling firm for instructions on disposal or replacement.

The recalled product

Product
HCG 2000 Units/mL Injection, packaged in a) 4 mL and b) 15 mL vials, Rx only, Essential Wellness PHARMACY, 4625 N. University, Peoria, IL 61614.
Manufacturer
Kalman Health & Wellness, Inc. dba Essential Wellness Pharma
Category
Drug — Injectable
Hazard
Affected units
2

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (4)

  • Lot #: 080415
  • Exp 09/04/2015
  • and 080715
  • Exp 09/07/2015

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 39 recalled by Kalman Health & Wellness, Inc. dba Essential Wellness Pharma under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 39 products in this recall →

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