Saluta (reduced Glutathione recalls

The FDA has published 1 recall involving Saluta (reduced Glutathione since 2014. The latest was reported on 21 May 2014. Most were for packaging defects. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls1since 2014

Last 12 months0reported

Class I00% of total

Ongoing0latest 21 May 2014

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

Why saluta (reduced glutathione is recalled

Packaging Defects1100%

Companies

Flawless Beauty1100%

By year

20141100%

All saluta (reduced glutathione recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
21 May 2014Drug	CLASS II	Saluta (reduced glutathione) Powder for Injection, 600 mg/vial recalled	Flawless Beauty	Packaging Defects	Nationwide

Should you stop taking Saluta (reduced Glutathione?

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.