The Recall Desk
SevereFDA (Drugs)·D-0148-2016·Announced 2015-11-04

Moses Lake Pharmacy Recalls TRIMIX Injectable Solution Due to Sterility Concerns

JD & SN Inc. is recalling 155 syringes of TRIMIX injectable solution nationwide due to a lack of assurance of sterility.

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. Per the rubric, FDA Class II recalls involving significant injury or property damage reports, or structural defects, are rated Severe (4). While no injuries are explicitly reported in the text, the lack of sterility assurance in an injectable drug represents a significant risk of harm, aligning with the Severe classification for Class II recalls with potential for serious harm.

Plain-English summary

JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling 155 syringes of TRIMIX, an injectable solution containing 20mg/1mg/20mcg/mL. The product is prescription-only and was distributed nationwide.

The recall was initiated due to a lack of assurance of sterility for all sterile human compounded drugs within their expiry dates. The source text does not specify reported illnesses or injuries associated with this recall.

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

The recalled product

Product
TRIMIX, injectable Solution, 20MG/1MG/20MCG/ML, 10mL 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 — Injectable Solution
Hazard
Affected units
155

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)

  • t11242014@14
  • t10082014@1
  • t08152014@22
  • t08042014@31
  • t07252014@19
  • t07142015@19
  • t07102015@24
  • t07082014@2
  • t04142015@25
  • t04062015@16
  • t02242015@29
  • 12152014@9
  • 12032014@4
  • 11122014@2
  • 10292014@3
  • 10012014@15
  • 09232014@23
  • 09032014@3
  • 08132014@1
  • 06242015@4

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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