The Recall Desk
ModerateFDA (Drugs)·D-0093-2021·Announced 2020-11-25

Milbar Recalls Willa Pore Perfector Pads Due to GMP Deviations

Milbar Laboratories is recalling 2,638 jars of Willa Pore Perfector pads due to Good Manufacturing Practice deviations. The product was distributed nationwide and internationally.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II due to GMP deviations, which typically indicates a reasonable probability of temporary or medically reversible adverse health consequences, fitting the Moderate severity criteria for voluntary precautionary recalls without reported serious injury.

Plain-English summary

Milbar Laboratories, Inc. is voluntarily recalling 2,638 plastic jars of Willa Pore Perfector (Salicylic Acid 2%) pads, 30 pads. The recall was initiated on October 9, 2020, and was classified as Class II by the FDA. The reason for the recall is Good Manufacturing Practice (GMP) deviations.

The affected product is identified by Lot # CW828-0 and an expiration date of Mar-22. The product was distributed throughout the United States, including Puerto Rico, and internationally. The recall was initiated by the firm and was terminated on January 4, 2023.

Consumers with this product should stop using it and contact the recalling firm for instructions on how to return the product or obtain a refund. The FDA classifies this as a Class II recall, meaning there is a reasonable probability that use of the product may cause temporary or medically reversible adverse health consequences.

The recalled product

Product
Willa Pore Perfector (Salicylic Acid 2%) pads, 30 pads
Manufacturer
Milbar Laboratories, Inc.
Category
Drug — Topical Medication
Hazard
Affected units
2,638

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • Lot #: CW828-0
  • Exp. Date Mar-22

Distribution

Distributed in 1 state:

Part of a larger recall action

This product is one of 14 recalled by Milbar Laboratories, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 14 products in this recall →

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Same hazard · gmp deviation

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