The Recall Desk
ModerateFDA (Drugs)·D-0116-2019·Announced 2018-11-07

Sprayology Recalls Party Relief Homeopathic Oral Spray Due to CGMP Deviations

Sprayology is recalling 2,956 bottles of Party Relief Homeopathic Oral Spray due to manufacturing conditions that could result in possible microbial contamination.

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 a theoretical risk of microbial contamination without reported illnesses, fitting the criteria for a voluntary precautionary recall or low-risk contamination.

Plain-English summary

Sprayology is voluntarily recalling 2,956 bottles of Party Relief, Homeopathic Oral Spray, 1.38 fl. oz (41ml). The product is identified by NDC 61096-0030-1 and Tester NDC 61096-1030-1. The recall covers all lots within their expiration dates.

The recall was initiated because the product was manufactured by a contract manufacturer under conditions that deviated from Current Good Manufacturing Practices (CGMP). These deviations could result in possible microbial contamination. The product was distributed nationwide in the USA.

Consumers who have this product should stop using it and contact Sprayology for further instructions or a refund.

The recalled product

Product
Party Relief, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0030-1 and Tester NDC 61096-1030-1
Manufacturer
Sprayology
Affected units
2,956

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 (1)

  • All lots within expiry

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 22 recalled by Sprayology 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 22 products in this recall →