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RECALLING FIRM / COMPANY

The Procter & Gamble Company Recalls

Are there any recent recalls involving The Procter & Gamble Company?

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.

7 FDA product recordsLatest initiation: Feb 1, 2024

Same product name.
Different batch.
Check the label.

Latest recalls involving The Procter & Gamble Company

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

Feb 1, 2024 · FDA status: TerminatedMeta Psyllium Fiber Capsules packaged as 100 count or 160 count PET bottles -…Illegible LabelView recall details →Jul 12, 2022 · FDA status: TerminatedVicks Children's Botanicals Liquid Daytime/Nighttime Combo Pack 4oz plastic…Acidified/Low Acid dietary supplement with no approved process.View recall details →Jul 12, 2022 · FDA status: TerminatedVicks Children's Botanicals Liquid Daytime 4oz plastic bottleAcidified/Low Acid dietary supplement with no approved process.View recall details →

Earlier recall history

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

2024 (1)2022 (6)

All recall records involving The Procter & Gamble Company

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

7 recall recordsPage 1 of 1
Class II
FDA status: Terminated

Meta Psyllium Fiber Capsules packaged as 100 count or 160 count PET bottles - 12 bottles per case.

Illegible Label

OtherView details →
Class II
FDA status: Terminated

Vicks Children's Botanicals Liquid Daytime/Nighttime Combo Pack 4oz plastic bottles

Acidified/Low Acid dietary supplement with no approved process.

OtherView details →
Class II
FDA status: Terminated

Vicks Children's Botanicals Liquid Daytime 4oz plastic bottle

Acidified/Low Acid dietary supplement with no approved process.

OtherView details →
Class II
FDA status: Terminated

Vicks Children's Botanicals Liquid Nighttime 4oz plastic bottle

Acidified/Low Acid dietary supplement with no approved process.

OtherView details →
Class II
FDA status: Terminated

Vicks ZzzQuil Liquid Melatonin Syrup Pediatric 8oz plastic bottle sold as single and twin pack

Acidified/Low Acid dietary supplement with no approved process.

OtherView details →
Class II
FDA status: Terminated

Vicks ZzzQuil Liquid Melatonin Syrup Adult 8oz plastic bottle sold as single and twin pack

Acidified/Low Acid dietary supplement with no approved process.

OtherView details →
Class II
FDA status: Terminated

Align Digestive De-Stress Capsules 21ct bottle packaged in paper carton 12 cartons per case

Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.

OtherView details →

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Same product name. Different batch. Details matter.

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