Honeywell eyesaline Eyewash Sterile Isotonic Solution — Class I drug recall D-0216-2017
Terminated recall by Sperian Eye & Face Protection, Inc, reported 2016-12-28, distributed nationwide. Non Sterility; contaminated with Klebsiella pneumoniae
| Recall number | D-0216-2017 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sperian Eye & Face Protection, Inc, Platteville, WI, United States |
| Recall initiated | 2016-08-16 |
| Classified | 2016-12-22 |
| Reported by FDA | 2016-12-28 |
| Terminated | 2019-05-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, MX |
| Quantity | 9,744 bottles |
| Reason classes | sterility |
| Lot numbers | F16091-61 |
| Expiration dates | 2019-03 |
Product
Honeywell eyesaline Eyewash Sterile Isotonic Solution, sterile water 99%, 32 fl. oz. (946 ml.), Sperian Eye & Face Protection, Inc. (a Honeywell Company), Platteville, WI 53818
Reason for recall
Non Sterility; contaminated with Klebsiella pneumoniae
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-0216-2017. 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.