Data Foundry

Drug recalls 2018

Toothette Short Term Oral Swab System with Perox-A-Mint Solution — Class II drug recall D-0355-2018

Terminated recall by Sage Products Inc, reported 2018-02-21, distributed nationwide. Cross Contamination With Other Products: Oral care solutions were manufactured by a third party supplier on eq

Recall numberD-0355-2018
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmSage Products Inc, Cary, IL, United States
Recall initiated2017-08-22
Classified2018-02-09
Reported by FDA2018-02-21
Terminated2018-12-13
DistributedNationwide (US)
Countries outside the USCA, GB, IE, NL, NZ
Quantity966 cases
UPC / GTIN / UDI-DI00618029820921
Lot numbers52149, 52982, 53942, 54042, 54925, 54952, 54958, 54959, 54962, 55872, 57449, 58381, 59302, 59765, 61788, 61831
Expiration dates2017-08-04, 2017-09-21, 2018-01-19, 2018-03-08, 2018-04-25, 2018-08-25, 2018-09-14, 2018-09-22, 2018-11-22, 2019-02-14

Product

Toothette Short Term Oral Swab System with Perox-A-Mint Solution. Contains: 20 Individually wrapped Toothette Plus Oral Swabs with sodium bicarbonate, 1.5 fl.oz/44mL bottle of Perox-A-Mint solution and One (1) 0.5 oz/14g tube of Mouth Moisturizer, Sage Products, Inc., 3909 Three Oaks Road, Cary, IL 60013. Product Code 6002 UPC (01)00618029820921

Reason for recall

Cross Contamination With Other Products: Oral care solutions were manufactured by a third party supplier on equipment shared with non-pharmaceutical products

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0355-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.