Check the Batch

RECALLING FIRM / COMPANY

Progressive Laboratories, Inc Recalls

Are there any recent FDA recalls involving Progressive Laboratories, 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.

4 FDA product recordsLatest initiation: Feb 23, 2018

Same product name.
Different batch.
Check the label.

All FDA recall records involving Progressive Laboratories, Inc

Initiated in 2018. Latest and historical records, ordered by initiation date (newest first). FDA status appears on each record.

4 recall recordsPage 1 of 1
Class I
FDA status: Terminated

Testosterzone 180 count bottle packaged in an amber plastic bottle with a black cap

Recalled dietary supplements may contain undeclared milk.

Undeclared allergenView details →
Class I
FDA status: Terminated

Thyroid Resilience 120 count bottle packaged in an amber plastic bottle with black cap

Recalled dietary supplements may contain undeclared milk.

Undeclared allergenView details →
Class I
FDA status: Terminated

Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white cap

Recalled dietary supplements may contain undeclared milk.

Undeclared allergenView details →
Class I
FDA status: Terminated

Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap

Recalled dietary supplements may contain undeclared milk.

Undeclared allergenView details →

Found your product? Now check the codes.

Same product name. Different batch. Details matter.

→