The Recall Desk
ModerateFDA (Drugs)·D-0084-2021·Announced 2020-11-25

Milbar Recalls DCL B Prox10 Anti-Blemish Wash Due to GMP Deviations

Milbar Laboratories is voluntarily recalling 7,591 bottles of DCL B Prox10 Anti-Blemish Wash due to Good Manufacturing Practice (GMP) deviations.

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 and is a voluntary precautionary recall due to GMP deviations, which aligns with the 'Moderate' severity criteria for low-risk contamination or voluntary actions without reported illness.

Plain-English summary

Milbar Laboratories, Inc. is voluntarily recalling 7,591 bottles of DCL B Prox10 Anti-Blemish Wash (Benzoyl Peroxide 10%), 200 ml/6.7 fl.oz. 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 the following lot numbers and expiration dates: Lot # MV098-4 (Exp. Date Dec-21), Lot # JW995 (Exp. Date Sep-22), and Lot # Fx381 (Exp. Date Jun-23). The product was distributed throughout the United States, including Puerto Rico, and internationally.

Consumers who have this product should stop using it and contact Milbar Laboratories, Inc. for further instructions. The recall status is currently terminated.

The recalled product

Product
DCL B Prox10 Anti-Blemish Wash (Benzoyl Peroxide 10%), 200 ml/6.7 fl.oz. Dermatologic Cosmetic Laboratories, East Haven, CT 06512 USA, UPC 0357486500853
Manufacturer
Milbar Laboratories, Inc.
Category
Drug — Topical Dermatologic
Hazard
Affected units
7,591

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 (4)

  • Lot # MV098-4
  • Exp. Date Dec-21 Lot #: JW995
  • Exp. Date Sep-22 Lot #: Fx381
  • Exp. Date Jun-23

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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