Trimix recalls

The FDA has published 35 recalls involving Trimix since 2012. The latest was reported on 18 Jan 2023. Most were for sterility. Tri-Coast Pharmacy has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls35since 2012
Last 12 months0reported
Class I00% of total
Ongoing12latest 18 Jan 2023

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 35 100%Class III 0 0%

Why trimix is recalled

By year

Ongoing trimix recalls

12 active

All trimix recalls, newest first

35 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IITriMix Plus 001 (PGE1/Papaverine HCl/Phentolamine Mesylate) recalledNorthern VA Compounders PllcSterilityNationwide
DrugCLASS IITriMix Plus 002 (PGE1/Papaverine HCl/Phentolamine recalledNorthern VA Compounders PllcSterilityNationwide
DrugCLASS IITrimix 30MG/1MG/10MCG/ML INJ in vials Assurance Infusion recalledAssurance InfusionSterilityNationwide
DrugCLASS IITrimix 30mg/1 mg/10mcg/mL ( 30 mg Papaverine recalledPharm D SolutionsSterilityNationwide
DrugCLASS IITriMix, Alprostadil/Phentolamine/Papaverine recalledTri-Coast PharmacySterilityNationwide
DrugCLASS IITrimix Injectable 30 mg/3 mg/60 mcg/mL, a), b) and c) vials recalledWells Pharmacy NetworkSterilityNationwide
DrugCLASS IITrimix Injectable 17.65 mg/0.59 mg/5.9 mcg/mL a), b) recalledWells Pharmacy NetworkSterilityNationwide
DrugCLASS IITriMix, Alprostadil/Phentolamine/Papaverine recalledTri-Coast PharmacySterilityNationwide
DrugCLASS IITrimix with Atropine Injectable 30 mg/3 mg/150 mcg/0.2 recalledWells Pharmacy NetworkSterilityNationwide
DrugCLASS IITriMix, Alprostadil/Phentolamine/Papaverine recalledTri-Coast PharmacySterilityNationwide
DrugCLASS IITrimix Injectable 30 mg/3 mg/100 mcg/mL, a) and vials recalledWells Pharmacy NetworkSterilityNationwide
DrugCLASS IITrimix Injectable 30 mg/2 mg/40 mcg vial recalledWells Pharmacy NetworkSterilityNationwide
DrugCLASS IITriMix, Alprostadil/Phentolamine/Papaverine recalledTri-Coast PharmacySterilityNationwide
DrugCLASS IITrimix with Atropine Injectable 30 mg/3 mg/60 mcg/0.2 mg/mL recalledWells Pharmacy NetworkSterilityNationwide
DrugCLASS IITriMix, Alprostadil/Phentolamine/Papaverine recalledTri-Coast PharmacySterilityNationwide
DrugCLASS IITriMix, Alprostadil/Phentolamine/Papaverine recalledTri-Coast PharmacySterilityNationwide
DrugCLASS IITriMix, Alprostadil/Phentolamine/Papaverine recalledTri-Coast PharmacySterilityNationwide
DrugCLASS IITriMix, Alprostadil/Phentolamine/Papaverine recalledTri-Coast PharmacySterilityNationwide
DrugCLASS IITriMix, Alprostadil/Phentolamine/Papaverine recalledTri-Coast PharmacySterilityNationwide
DrugCLASS IITriMix, Alprostadil/Phentolamine/Papaverine recalledTri-Coast PharmacySterilityNationwide
DrugCLASS IITriMix, Alprostadil/Phentolamine/Papaverine recalledTri-Coast PharmacySterilityNationwide
DrugCLASS IITrimix with Atropine Injectable 30 mg/3 mg/300 mcg/0.2 recalledWells Pharmacy NetworkSterilityNationwide
DrugCLASS IITrimix Injectable 30 mg/1 mg/25 mcg/mL vial recalledWells Pharmacy NetworkSterilityNationwide
DrugCLASS IITrimix Injectable 30 mg/1 mg/10 mcg/mL a) and b) recalledWells Pharmacy NetworkSterilityNationwide
DrugCLASS IITrimix Injectable 30 mg/2 mg/20 mcg, a) and b) vials recalledWells Pharmacy NetworkSterilityNationwide
DrugCLASS IITriMix, Alprostadil/Phentolamine/Papaverine recalledTri-Coast PharmacySterilityNationwide
DrugCLASS IITrimix, injectable Solution, 20MG/1MG/20MCG/ML syringe recalledJD & SN IncSterilityNationwide
DrugCLASS IITrimix, injectable Solution, 40MG/2MG/40MCG/ML, syringe size recalledJD & SN IncSterilityNationwide
DrugCLASS IITrimix, injectable Solution, 15MG/.5MG/5MCG/ML syringe recalledJD & SN IncSterilityNationwide
DrugCLASS IITrimix, injectable Solution, 30MG/1MG/10MCG, syringe sizes recalledJD & SN IncSterilityNationwide

Should you stop taking Trimix?

Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.