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RECALLING FIRM / COMPANY

GMP Laboratories of America Inc Recalls

Are there any recent recalls involving GMP Laboratories of America Inc?

0 recall records initiated in the snapshot’s last 365 days. 0 are FDA-listed ongoing with no termination date.FDA data updated September 16, 2026 · Snapshot assessed September 18, 2026

The FDA identifies this company as the recalling firm; this does not establish that it is the manufacturer, retailer or brand owner. “Recent ongoing” means initiated within 365 days of September 18, 2026, FDA status “Ongoing,” and no termination date. This snapshot cannot confirm what is active today.

3 FDA product recordsLatest initiation: Jun 24, 2025

Same product name.
Different batch.
Check the label.

Latest recalls involving GMP Laboratories of America Inc

Most recently initiated in the available FDA data; these are not necessarily active recalls.

Jun 24, 2025 · FDA status: TerminatedLithium Orotate 2.5; 60 vegetarian capsules, Dietary SupplementDownstream recall of a dietary supplement ingredient that was manufactured out of specifications.View recall details →Jun 24, 2025 · FDA status: TerminatedLithium Orotate, Weyland Brain Nutrition ; 60 vegetarian capsules, Dietary…Downstream recall of a dietary supplement ingredient that was manufactured out of specification.View recall details →Dec 8, 2009 · FDA status: TerminatedDietary supplement. Product is labeled as :" Rescue Me***911 Damage…The firm recalled because the product lot contained mispackaged product wherein some capsules were missing from the finished packaged product.View recall details →

Earlier recall history

3 records initiated before 2026. Browse the history below or choose a year.

2025 (2)2009 (1)

All recall records involving GMP Laboratories of America Inc

Latest and historical records, ordered by initiation date (newest first). FDA status appears on each record.

3 recall recordsPage 1 of 1
Class III
FDA status: Terminated

Lithium Orotate 2.5; 60 vegetarian capsules, Dietary Supplement

Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.

OtherView details →
Class III
FDA status: Terminated

Lithium Orotate, Weyland Brain Nutrition ; 60 vegetarian capsules, Dietary Supplement

Downstream recall of a dietary supplement ingredient that was manufactured out of specification.

OtherView details →
Class II
FDA status: Terminated

Dietary supplement. Product is labeled as :" Rescue Me***911 Damage Control***brantley living herbal formulas***HERBAL…

The firm recalled because the product lot contained mispackaged product wherein some capsules were missing from the finished packaged product.

OtherView details →

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Same product name. Different batch. Details matter.

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