The Recall Desk
SevereFDA (Drugs)·D-0122-2016·Announced 2015-11-04

Moses Lake Pharmacy Recalls Sermorelin Injectable Solution Due to Sterility Concerns

Moses Lake Professional Pharmacy is recalling 41 syringes of Sermorelin/GHRP-6/GHRP-2 injectable solution because the FDA cannot assure the sterility of the compounded drug.

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 recall is classified as FDA Class II, which corresponds to a Severe severity score under the rubric, particularly given the risk of infection associated with non-sterile injectable drugs.

Plain-English summary

JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling 41 syringes of Sermorelin/GHRP-6/GHRP-2, Injectable Solution, 9/9/9MG/9ML. The recall was initiated because the FDA cannot assure the sterility of the sterile human compounded drugs within their expiry dates.

The affected product is a prescription-only injectable solution distributed nationwide. The recall covers specific lots identified by codes such as t12052014@8 and 10222014@8.

Consumers who have this product should stop using it and contact their healthcare provider or the pharmacy for further instructions.

The recalled product

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
Manufacturer
JD & SN Inc., dba Moses Lake Professional Pharmacy
Category
Drug — Compounded Injectable
Hazard
Affected units
41

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 (19)

  • 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.

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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