The Recall Desk

FDA (Drugs) recall action 71806

JD & SN Inc., dba Moses Lake Professional Pharmacy recalled 101 products on 2015-11-04

The FDA (Drugs) publishes a recall like this one as 101 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 101 pages.

Products
101
Announced
2015-11-04
Critical
0
Units
3,535

Why these products were recalled

Lack of Assurance of Sterility; all sterile human compounded drugs within expiry

The agency’s own wording, quoted from the enforcement report.

The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.

101–101 of 101

  • SevereFDA (Drugs)··2015-11-04

    FDA Recalls Testosterone Cypionate Injection Due to Sterility Concerns

    FDA is recalling Testosterone Cypionate for SubQ Injection from Moses Lake Professional Pharmacy due to lack of assurance of sterility.

    Product
    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
    Category
    Distribution
    0 states