Gaba recalls

The FDA has published 2 recalls involving Gaba since 2013. The latest was reported on 20 Jul 2016. Most were for sterility. Medaus 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 recalls2since 2013

Last 12 months0reported

Class I00% of total

Ongoing1latest 20 Jul 2016

Recalls per month, last 24 months

click a bar for that month

0Dec '24 0 0 0Mar 0 0 0Jun 0 0 0Sep 0 0 0Dec 0 0 0Mar 0 0 0Jun 0 0 0Sep 0 0

Severity split

Class I 0 0%Class II 2 100%Class III 0 0%

Why gaba is recalled

Sterility2100%

Companies

Medaus150%
Lowlite Investments150%

By year

2016150%
2013150%

Ongoing gaba recalls

1 active

Reported	Class	Recall	Company	Reason	Where
17 Jul 2013Drug	CLASS II	Gaba 50 mg/Mag Sulfate 50 mg/Taurine/Theanine 50 mg/ml recalled	Lowlite Investments	Sterility	Nationwide

All gaba recalls, newest first

2 total

Reported	Class	Recall	Company	Reason	Where
20 Jul 2016Drug	CLASS II	Gaba 50MG/ML (PF) Vials, Medaus Pharmacy recalled	Medaus	Sterility	Nationwide
17 Jul 2013Drug	CLASS II	Gaba 50 mg/Mag Sulfate 50 mg/Taurine/Theanine 50 mg/ml recalled	Lowlite Investments	Sterility	Nationwide

Should you stop taking Gaba?

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.