HILLYARD — Class II drug recall D-140-2013
Terminated recall by Hillyard GMP, reported 2013-02-06, distributed nationwide. Microbial Contamination of Non-Sterile Products: The product may be contaminated with bacteria.
| Recall number | D-140-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hillyard GMP, Saint Joseph, MO, United States |
| Recall initiated | 2012-12-28 |
| Classified | 2013-01-31 |
| Reported by FDA | 2013-02-06 |
| Terminated | 2014-01-29 |
| Distributed | Nationwide (US) |
| Quantity | 2,139 bottles |
| Reason classes | microbial contamination, sterility |
| NDC | 76402-0403, 76402-0403-02, 76402-0403-03, 76402-0403-06, 76402-0403-82 |
| Lot numbers | 03/14, 09/14, 1025554, 1030652 |
Product
HILLYARD, Alcohol Free Foaming Instant Hand Sanitizer, Benzalkonium Chloride 0.10%, 1.25 L plastic bottle, OTC, HILLYARD IDUSTRIES, St. Joseph, MO. 64502 NDC 76402-403-03
Reason for recall
Microbial Contamination of Non-Sterile Products: The product may be contaminated with bacteria.
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-140-2013. 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.