Honeywell Eyewash Solution Recall: Contaminated with Klebsiella pneumoniae
Sperian Eye & Face Protection recalls Honeywell eyewash solution due to contamination with Klebsiella pneumoniae. Affected lots may cause infection if used.
Lower-risk recall
Non Sterility; contaminated with Klebsiella pneumoniae
Contact the company
What happened, in plain English
Sperian Eye & Face Protection is recalling Honeywell eyewash solution because it was contaminated with Klebsiella pneumoniae bacteria. Using this product could lead to eye infections. Read more at govinfonow.com/recall/42485-honeywell-eyewash-solution-recall-contaminated-with-klebsiella-pneumoniae.
Source Summary by GovInfoNow · govinfonow.com/recall/42485-honeywell-eyewash-solution-recall-contaminated-with-klebsiella-pneumoniae · Updated October 9, 2026 · FDA enforcement record: FDA #D-0216-2017
Cite this page
“Honeywell Eyewash Solution Recall: Contaminated with Klebsiella pneumoniae.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/42485-honeywell-eyewash-solution-recall-contaminated-with-klebsiella-pneumoniae. Based on FDA recall #D-0216-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0216-2017%22&limit=1).
Why it’s dangerous
The eyewash solution was contaminated with Klebsiella pneumoniae bacteria during manufacturing. This can cause eye infections, especially if the solution is used for cleaning eyes.
Who’s affected
People who own or use the recalled eyewash solution for eye cleaning. Those with compromised immune systems may be at higher risk.
How to tell if you have this one
Check for lot number F16091-61 with expiration date 03/2019. The product codes include 32-000455-0000-H5, 32-000455-0036, 32-000461-0036, 32-000462-0000-H5, and 32-000462-0036.
- Brand
Sperian Eye & Face- Category
Drug
What to do — step by step
Check Product Lot Number
Look for lot number F16091-61 with expiration date 03/2019 on the product label.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Nationwide. Outside the US to include: Australia, Mexico and United Arab Emirates.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 2.8 years after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0216-2017 (August 16, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0216-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.