Agency classClass IIOur severity:Severe FDA (Drugs)·D-0151-2016·Announced 2015-11-04

Moses Lake Pharmacy Recalls Trimix Injectable Solution Due to Sterility Concerns

Moses Lake Professional Pharmacy is recalling Trimix injectable solution because the FDA cannot assure the sterility of the compounded drug.

The agency’s classification

FDA (Drugs): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. 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 with potential for hospitalization or significant injury are rated as Severe (4).

Plain-English summary

JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling 10 syringes of TRIMIX, injectable Solution, 30MG/2MG/20MCG. 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 including t12102014@2, t11212014@14, and others listed in the official notice.

Consumers who have this product should stop using it and contact their healthcare provider or the pharmacy for further instructions. The recall is classified as FDA Class II, indicating a reasonable probability that use of the product may cause temporary or medically reversible health consequences.

The recalled product

Product: TRIMIX, injectable Solution, 30MG/2MG/20MCG, syringe size: 10mL, 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: sterility
infection
Affected units: 10

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 (11)

t12102014@2
t11212014@14
t11102014@22
t11072014@10
t10102014@20
t08072014@37
t06222015@13
t06192015@27
t06112015@23
t04142015@9
t02272015@26.

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 →

Same manufacturer · JD & SN Inc., dba Moses Lake Professional Pharmacy

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Same hazard · sterility