Morphine-bupivacaine-ketamine Pf Syringe recalls

The FDA has published 1 recall involving Morphine-bupivacaine-ketamine Pf Syringe since 2021. The latest was reported on 18 Aug 2021. Most were for sterility. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls1since 2021

Last 12 months0reported

Class I1100% of total

Ongoing0latest 18 Aug 2021

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 1 100%Class II 0 0%Class III 0 0%

Why morphine-bupivacaine-ketamine pf syringe is recalled

Sterility1100%

Companies

Med Shop Total Care1100%

By year

20211100%

All morphine-bupivacaine-ketamine pf syringe recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
18 Aug 2021Drug	CLASS I	Morphine-bupivacaine-ketamine PF Injectable syringe recalled	Med Shop Total Care	Sterility	PR, TX

Should you stop taking Morphine-bupivacaine-ketamine Pf Syringe?

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.