Recalls / Class II
Class IID-0122-2016
Product
SERMORELIN/GHRP-6/GHRP-2, Injectable Solution, 9/9/9MG/9ML, 9 mL syringe, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
- Affected lot / code info
- t12052014@8, t11192014@26, t11032014@24, t10142014@27, t09172014@2, t08252014@30, t07302014@12, t07092014@15, t06022015@10, t04302015@22, t03312015@18, t03172015@28, t03092015@38, t02102015@21, 10222014@8, 10012014@16, 05132015@5, 02172015@7, 01052015@9.
Why it was recalled
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recalling firm
- Firm
- JD & SN Inc., dba Moses Lake Professional Pharmacy
- Notification channel
- Press Release
- Type
- Voluntary: Firm initiated
- Address
- 1555 Pilgrim St, N/A, Moses Lake, Washington 98837-4623
Distribution
- Quantity
- 41 syringes
- Distribution pattern
- Nationwide
Timeline
- Recall initiated
- 2015-07-24
- FDA classified
- 2015-10-27
- Posted by FDA
- 2015-11-04
- Terminated
- 2016-04-13
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-0122-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.