CHORIONIC GONADOTROPIN, Injectable Solution,175 UNITS/1.5mg per syringe with Methylcobalamin, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

Class I - Dangerous
💊 Drugs Recalled: July 24, 2015 JD & SN Inc. Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    04292015@12, 05042015@8, 05202015@21, 06102015@25, 06242015@14, 07012015@8, 07062015@21, t03062015@15, t03122015@33, t03182015@45, t03192015@2, t04082015@14, t04082015@3, t04202015@22, t05082015@27, t05192015@29, t06022015@37, and t07152015@5.
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
JD & SN Inc., dba Moses Lake Professional Pharmacy
Reason for Recall:
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

CHORIONIC GONADOTROPIN, Injectable Solution,175 UNITS/1.5mg per syringe with Methylcobalamin, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

Product Codes/Lot Numbers:

04292015@12, 05042015@8, 05202015@21, 06102015@25, 06242015@14, 07012015@8, 07062015@21, t03062015@15, t03122015@33, t03182015@45, t03192015@2, t04082015@14, t04082015@3, t04202015@22, t05082015@27, t05192015@29, t06022015@37, and t07152015@5.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0063-2016

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