Reported Nov 13, 2019 · Terminated

S-TRIMIX various strengths to include:a) S-TRIMIX (15MG/1MG/10MCG/ML) MDV: b) S-TRIMIX (18MG/0.6MG/6MCG/ML) MDV INJ: c)…

First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy · 6828 E Brown Rd Ste 101 · Mesa, AZ · 85207-3761

S-TRIMIX various strengths to includea)
S-TRIMIX (15MG/1MG/10MCG/ML) MDVb) S-TRIMIX (18MG/0.6MG/6MCG/ML)
MDV INJc) S-TRIMIX (24MG/0.89MG/8.9MCG/ML)
MDV INJd) S-TRIMIX (28.85MG/1.9MG/19.2MCG/ML)
MDVe)
S-TRIMIX (30MG/1MG/10MCG/ML) MDVf)
S-TRIMIX (30MG/2MG/25MCG/ML) MDVg)
S-TRIMIX (40MG/3MG/39MCG/ML) MDV INJh) S-TRIMIX (PA 60MG/PH 1.25MG/PG 6MCG/ML)
MDV INJi) S-TRIMIX HYOCTANE (29.4MG/1MG/9MCG/ML) j) S-TRIMIX III (29.4MG/0.98MG/9.8MCG/ML)
INJk) S-TRIMIX STD (16.67MG/0.58MG/8.88MCG/ML)
INJl)
S-TRIMIX-104 (30MG/2MG/20MCG/ML) MDVm) S-TRIMIX-DS (16.67MG/0.58MG/17.7MCG/ML)
MDVRx Only, 5ml glass vial. Red Mountain Compounding Rx

Lot codes and dates: 14 of 14 products
Products covered by this recall
# Product as published
1 Lot #:a) S07162019DH@07, EXP. 9/16/19 b) S06242019DH@01, EXP 8/24/19
2 S07102019DT@15, EXP. 9/20/19
3 S07252019DH@03, EXP. 9/25/19
4 S07312019DH@13, EXP. 9/31/19 c) S07102019DT@03, EXP. 9/10/19 d) S07262019DH@01, EXP. 9/26/19
5 S07232019DH@07, EXP. 9/23/19 e) S06262019DH@05, EXP. 8/26/19
6 S07132019DT@06, EXP. 9/13/19 f) S06162019DH@12, EXP. 8/16/19 g) S06252019DT@06, EXP. 8/25/19
7 S07032019DT@04, EXP. 9/3/19
8 S07102019DT@02, EXP. 9/10/19
9 S07172019dt@13, EXP. 9/17/19 i) S07032019DT@01, EXP. 9/3/19 j) S06092019DH@07, EXP. 8/9/19
10 S06112019DH@03, EXP. 8/11/19
11 S06122019DT@01, EXP. 8/12/19 k) S07022019DT@05, EXP. 9/2/19
12 S07132019DT@04, EXP. 9/13/19 l) S07022019DT@01, EXP. 9/2/19
13 S07302019DH@06, EXP. 9/30/19 m) S06252019DT@07, EXP. 8/25/19
14 S07022019DT@04, EXP. 9/2/19
Amount recalled: 34x5ml glass vial

The agency filed one notice per product. You are reading one of them; the other 99 are below.

87 more are in the archive.

Lack of Assurance of Sterility

This product could cause temporary or reversible health problems — stop using it.

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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