FDA recall record

Church & Dwight Orajel Baby, Cooling Swabs for Teething, Each Unit 0.007 fl oz (0.22 mL) recall — FDA D-0506-2025

Microbial Contamination of Non-Sterile Products: Fungal contamination of infant oral swabs.

Class Iclassification
D-0506-2025official record ID
Jul 9, 2025report date

Recall record at a glance

Official recordD-0506-2025
CategoryDrug Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmChurch & Dwight Inc
Report dateJul 9, 2025
Recall initiation dateJun 6, 2025
Quantity695,880 cartons
LocationPrinceton, NJ, United States

Official product description

Orajel Baby, Cooling Swabs for Teething, Each Unit 0.007 fl oz (0.22 mL), NET 0.08 FL OZ (2.6 mL) TOTAL, 12 Single-Use Swabs per carton, Manufactured for Church & Dwight Co. Inc. Ewing. NJ 08328 USA. UPC CODE 3 10310 40000 2.

Why the product was recalled

Microbial Contamination of Non-Sterile Products: Fungal contamination of infant oral swabs.

Distribution information

Nationwide in the USA.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.