The Recall Desk
SevereFDA (Drugs)·D-0505-2025·Announced 2025-07-09

Zicam Nasal AllClear swabs recalled over fungal contamination of swabs

Zicam Nasal AllClear swabs are being recalled because of fungal contamination of the nasal swabs. All lots are affected, covering 13,632 cartons.

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: FDA Class I recall, which the rubric floors at Severe; no illness is reported in the source, so it does not escalate to Critical.

Plain-English summary

Zicam Nasal AllClear, 20 single-use swabs per carton, distributed by Church & Dwight Co., Inc. of Ewing, New Jersey, UPC 7 32216 30165 6, is being recalled. The action covers 13,632 cartons and applies to all lots.

The stated reason is microbial contamination of non-sterile products: fungal contamination of the nasal swabs. The FDA classified the action as Class I, its most serious classification.

Distribution was nationwide in the USA. The product is sold over the counter.

Consumers who have the product should stop using it and follow the instructions issued by the distributor. Anyone who has used it and feels unwell should seek medical advice.

The recalled product

Product
ZICAM NASAL ALLCLEAR, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc.., Ewing NJ. UPC 7 32216 30165 6
Affected units
13,632

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.

Part of a larger recall action

This product is one of 3 recalled by Church & Dwight 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 3 products in this recall →