The Recall Desk
SevereFDA (Drugs)·D-0470-2016·Announced 2015-12-09

Western Drug Recalls Wilson's Nasal Irrigation Solution Due to Sterility Concerns

Western Drug is recalling Wilson's Nasal Irrigation Solution because the product lacks assurance of sterility. The recall affects two containers distributed nationwide.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The agency classification is FDA Class II. According to the rubric, FDA Class II recalls with potential for significant injury or hospitalization (implied by sterility failure in a medical context) map to a score of 4 (Severe), as Class I is required for a score of 5.

Plain-English summary

Western Drug Inc. is recalling Wilson's Nasal Irrigation Solution, a prescription product, due to a lack of assurance of sterility. The recall involves two containers of the product.

The affected product was distributed nationwide in the United States, specifically in Arizona, California, Georgia, New Mexico, South Carolina, South Dakota, Texas, and Utah. All lots of the product are included in this recall.

Consumers who have this product should stop using it and contact their healthcare provider or the recalling firm for further instructions. The FDA has classified this recall as Class II, indicating that use of the product could cause temporary or medically reversible health consequences.

The recalled product

Product
Wilson's Nasal Irrigation Solution, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
Manufacturer
Western Drug
Affected units
2

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

Distribution

Distributed nationwide across the United States.

The notice also names 8 states specifically:

Part of a larger recall action

This product is one of 91 recalled by Western Drug 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 91 products in this recall →