The Recall Desk
ModerateFDA (Drugs)·D-0846-2016·Announced 2016-05-18

Sesderma Dryses Deodorant Recalled for cGMP Deviations

Sesderma is recalling Dryses Aluminum Chlorohydrate Deodorant for Men because the product does not comply with cGMP requirements.

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 involves cGMP deviations without reported illnesses or injuries, fitting the criteria for a moderate severity voluntary precautionary recall.

Plain-English summary

Sesderma, SL is recalling 354 bottles of Dryses Aluminum Chlorohydrate Deodorant for Men Roll-on, 2.5 fl oz (75 mL). The product is an over-the-counter deodorant manufactured in Valencia, Spain. The recall is due to cGMP deviations, meaning the product does not comply with current Good Manufacturing Practice requirements.

The affected product is identified by NDC 63181-0019-1 and UPC 8 470002 075221. Specific lot codes and expiration dates include Lot 40414701 (exp 09/19), Lot 33524701 (exp 10/18), and Lot 40144101 (exp 10/18). The product was distributed to Florida, Puerto Rico, Colorado, and Georgia.

Consumers with this product should stop using it and contact Sesderma, SL for further instructions.

The recalled product

Product
Dryses Aluminum Chlorohydrate Deodorant for Men Roll-on, 2.5 fl oz (75 mL) bottle, over the counter, Manufactured by Sesderma S.L., Valencia, Spain, NDC 63181-0019-1 UPC 8 470002 075221
Manufacturer
Sesderma, SL
Category
Drug — Deodorant
Hazard
Affected units
354

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 (5)

  • Lot code 40414701
  • exp 09/19
  • Lot code 33524701
  • exp 10/18
  • Lot code 40144101

Distribution

Distributed in 4 states:

Part of a larger recall action

This product is one of 10 recalled by Sesderma, SL 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 10 products in this recall →

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