Morphine (pf recalls

The FDA has published 8 recalls involving Morphine (pf since 2014. The latest was reported on 23 Feb 2022. Most were for sterility. Pharmakon Pharmaceuticals 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 recalls8since 2014

Last 12 months0reported

Class I113% of total

Ongoing0latest 23 Feb 2022

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 1 13%Class II 7 88%Class III 0 0%

Why morphine (pf is recalled

Companies

By year

2022113%
2016450%
2015113%
2014225%

All morphine (pf recalls, newest first

8 total

Reported	Class	Recall	Company	Reason	Where
23 Feb 2022Drug	CLASS I	Morphine Sulfate PF 25 mg/ (1 mg/mL) in NaCl in Single Dose Syringe recalled	Staq Pharma	Labeling Errors	CO, OH, TX
20 Jul 2016Drug	CLASS II	Morphine Sulfate (PF) 1mg/mL recalled by Pharmakon Pharmaceuticals	Pharmakon Pharmaceuticals	Sterility	Nationwide
20 Jul 2016Drug	CLASS II	Morphine Sulfate (PF) 0.5mg/mL recalled by Pharmakon Pharmaceuticals	Pharmakon Pharmaceuticals	Sterility	Nationwide
3 Feb 2016Drug	CLASS II	Morphine Sulfate (PF) 0.1 mg/mL in 0.9% Sodium Chloride, injectable recalled	Pharmakon Pharmaceuticals	Potency & Assay	Nationwide
3 Feb 2016Drug	CLASS II	Morphine Sulfate (PF) 0.5 mg/mL in 0.9% Sodium Chloride, injectable recalled	Pharmakon Pharmaceuticals	Potency & Assay	Nationwide
25 Nov 2015Drug	CLASS II	Morphine PF (2 mg/ Single Use Vial, For IV or IM Administration recalled	US Compounding	Sterility	Nationwide
5 Nov 2014Drug	CLASS II	Morphine sulfate (PF) 20 mg/mL injectable recalled	Martin Avenue Pharmacy	Sterility	Nationwide
5 Nov 2014Drug	CLASS II	Morphine sulfate (PF) 3 mg/mL injectable recalled	Martin Avenue Pharmacy	Sterility	Nationwide

Should you stop taking Morphine (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.