Midazolam (pf recalls

The FDA has published 3 recalls involving Midazolam (pf since 2016. The latest was reported on 20 Jul 2016. Most were for potency & assay. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls3since 2016

Last 12 months0reported

Class I00% of total

Ongoing0latest 20 Jul 2016

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 3 100%Class III 0 0%

Why midazolam (pf is recalled

Potency & Assay267%
Sterility133%

Companies

Pharmakon Pharmaceuticals3100%

By year

20163100%

All midazolam (pf recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
20 Jul 2016Drug	CLASS II	Midazolam (PF) 5mg/ml BD syringe recalled by Pharmakon Pharmaceuticals	Pharmakon Pharmaceuticals	Sterility	Nationwide
3 Feb 2016Drug	CLASS II	Midazolam (PF) 0.5 mg/mL in 0.9% Sodium Chloride, injectable recalled	Pharmakon Pharmaceuticals	Potency & Assay	Nationwide
3 Feb 2016Drug	CLASS II	Midazolam (PF) 0.1 mg/mL in 0.9% Sodium Chloride, injectable recalled	Pharmakon Pharmaceuticals	Potency & Assay	Nationwide

Should you stop taking Midazolam (pf?

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.