Reported Nov 7, 2018 · Terminated
Tri-Mix XL 150 mg/10 mg/100 mcg a) Injectable NDC 69699-1353-10; b) (LYO) Powder NDC 69699-1353-10, Pharm D Solutions,…
Pharm D Solutions, LLC
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: Pharm D Solutions, LLC · 1304 S Loop W · Houston, TX · 77054-4010
Is this the product you have?
- Tri-Mix XL 150 mg/10 mg/100 mcg a) Injectable NDC 69699-1353-10; b) (LYO) Powder NDC 69699-1353-10, Pharm D Solutions, Houston, Texas
- Lot codes and dates
- Lota) 04132018:97
- Discard by
10/10/201804032018:25
- Discard by9/30/2018
- b) 0416201829
- Discard by
10/11/201803282018:80
- Discard by
9/24/201806122018:06
- Discard by
12/9/201808132018:55
- Discard by2/9/2019
- Amount recalled
- 553 vials
This recall covers 79 products
The agency filed one notice per product. You are reading one of them; the other 78 are below.
66 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Lack of Assurance of Sterility
This product could cause temporary or reversible health problems — stop using it.
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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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