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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 97031

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
June 06, 2025
Product types
Drug
Classifications
Class I
Statuses
Ongoing
Recalling firm wording
Church & Dwight Inc

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 3

ZICAM COLD REMEDY MEDICATED NASAL SWABS, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc., Ewing NJ. UPC 7 32216 30120 5

D-0504-2025
Recall number
D-0504-2025
Initiated
June 06, 2025
Classification
Class I
Status
Ongoing
Recalling firm
Church & Dwight Inc
Quantity
3,374,918 cartons

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
Microbial Contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

All lots.

Distribution pattern

Nationwide in the USA.

drug · product 2 of 3

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

D-0505-2025
Recall number
D-0505-2025
Initiated
June 06, 2025
Classification
Class I
Status
Ongoing
Recalling firm
Church & Dwight Inc
Quantity
13,632 cartons

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
Microbial Contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

All Lots.

Distribution pattern

Nationwide in the USA.

drug · product 3 of 3

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.

D-0506-2025
Recall number
D-0506-2025
Initiated
June 06, 2025
Classification
Class I
Status
Ongoing
Recalling firm
Church & Dwight Inc
Quantity
695,880 cartons

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
Microbial Contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

All Lots.

Distribution pattern

Nationwide in the USA.

Field note

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