TESTOSTERONE CYPIONATE FOR SUBQ INJECTION, Injectable Solution, 200 mg/mL, syringe size: 5ml and 10mL, 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:
    t12312014@11, t10302014@9, t08062014@28, t05292015@30, t04282015@12, t04092015@22, t03302015@1, t03102015@29, t02172015@2, t01292015@18, 12082014@10, 11242014@5, 11122014@5, 10222014@24, 10012014@19, 09242014@7, 09152014@17, 08152014@27, 08042014@6, 07112014@23, 07082015@8, 06172015@14, 05272015@12, 05132015@12, 04082015@1, 03092015@11, 02232015@2.
  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:

TESTOSTERONE CYPIONATE FOR SUBQ INJECTION, Injectable Solution, 200 mg/mL, syringe size: 5ml and 10mL, 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:

t12312014@11, t10302014@9, t08062014@28, t05292015@30, t04282015@12, t04092015@22, t03302015@1, t03102015@29, t02172015@2, t01292015@18, 12082014@10, 11242014@5, 11122014@5, 10222014@24, 10012014@19, 09242014@7, 09152014@17, 08152014@27, 08042014@6, 07112014@23, 07082015@8, 06172015@14, 05272015@12, 05132015@12, 04082015@1, 03092015@11, 02232015@2.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0143-2016

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