The Recall Desk
SevereFDA (Drugs)·D-0124-2016·Announced 2015-11-04

Moses Lake Professional Pharmacy Recalls Testosterone Pellets Due to Sterility Concerns

JD & SN Inc. is recalling 298 units of compounded testosterone pellets because the FDA cannot ensure the product is sterile.

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 agency classification is FDA Class II, and the hazard involves a lack of assurance of sterility in a compounded drug, which aligns with the criteria for Severe severity.

Plain-English summary

JD & SN Inc., doing business as Moses Lake Professional Pharmacy, is recalling 298 units of TESTOSTERONE, Pellet, 200 mg. The product is a prescription-only compounded drug distributed nationwide.

The recall was initiated due to a lack of assurance of sterility. The source text indicates that all sterile human compounded drugs within their expiry date are affected by this issue.

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

The recalled product

Product
TESTOSTERONE, Pellet, 200 mg, 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 Sterile Drug
Hazard
Affected units
298

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 (20)

  • 01202015@19
  • 05192015@3
  • 07222014@27
  • 08192014@4
  • 09042014@5
  • 09232014@21
  • 10032014@24
  • 10092014@12
  • 12012014@16
  • t01152015@6
  • t02232015@23
  • t03122015@1
  • t03202015@10
  • t04232015@11
  • t05062015@22
  • t05182015@29
  • t06012015@12
  • t06112015@10
  • t06132014@15
  • t08112014@30

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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