The Recall Desk
SevereFDA (Drugs)·D-0067-2016·Announced 2015-11-04

Moses Lake Pharmacy Recalls Compounded Chorionic Gonadotropin Due to Sterility Concerns

Moses Lake Professional Pharmacy is recalling compounded chorionic gonadotropin injectable solutions because the FDA cannot assure the sterility of the product.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The agency classification is FDA Class II, and the rubric specifies that FDA Class II recalls with potential for significant injury or structural defects (such as sterility issues in injectables) are classified as Severe.

Plain-English summary

JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling specific lots of CHORIONIC GONADOTROPIN COMPOUNDED, Injectable Solution. The product is packaged in 14, 26, and 40-count containers and is available by prescription only. The recall is being conducted because the FDA cannot assure the sterility of the compounded human drugs within their expiration dates.

The affected product was distributed nationwide. The recall includes specific lot codes ranging from 07092014 to 07132015, as listed in the structured product information. The total quantity involved is 1 (14-count) container, 1 (40-count) container, and 30 (26-count) containers.

Consumers who have this product should stop using it and contact their healthcare provider or the pharmacy for instructions on how to return or dispose of the medication. The FDA classifies this recall as Class II, indicating a reasonable probability that the use of the product could cause temporary or medically reversible health consequences.

The recalled product

Product
CHORIONIC GONADOTROPIN COMPOUNDED, Injectable Solution, 175 UNITS/0.175ML per syringe, packaged in 14, 26, and 40-count containers, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Manufacturer
JD & SN Inc., dba Moses Lake Professional Pharmacy
Category
Drug — Compounded Injectable
Hazard

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 (20)

  • 01052015@18
  • 01072015@12
  • 01122015@13
  • 01142015@7
  • 01192015@18
  • 01212015@16
  • 01262015@11
  • 02022015@13
  • 02192015@10
  • 02232015@22
  • 03042015@20
  • 03092015@46
  • 03162015@13
  • 03182015@17
  • 03252015@23
  • 03302015@13
  • 04012015@11
  • 04152015@14
  • 04212015@15
  • 04272015@13

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 101 recalled by JD & SN Inc., dba Moses Lake Professional Pharmacy 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 101 products in this recall →

Related recalls

Same manufacturer · JD & SN Inc., dba Moses Lake Professional Pharmacy

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Same hazard · sterility

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