Honeywell recalls saline eyewash solution cartridges due to CGMP deviations. Affected units contain 7.9 gallons and expire June 2025. No specific remedy is listed in the recall notice.
CGMP Deviations
Honeywell is recalling saline eyewash solution cartridges for the Fendall 2000 model due to regulatory deviations in manufacturing. This recall does not specify a remedy, so users should contact Honeywell directly for guidance.
CGMP deviations refer to failures in the manufacturing process that could lead to product quality issues. However, the recall does not specify what these deviations are or how they might affect safety.
Users of the Fendall 2000 eyewash system with the recalled saline solution cartridges are affected. Workers in industrial settings using these cartridges for eye safety are most at risk.
Check for the product name 'Eyesaline, Saline Eyewash Solution, Cartridge for Fendall 2000' with 7.9 gallons per cartridge. The expiration date is June 2025, and the NDC code is 0498-0631-37.
Reach out to Honeywell directly for specific instructions on handling the recalled product.
The recall notice does not specify a remedy.
The expiration date is June 2025.
Check for the product name 'Eyesaline, Saline Eyewash Solution, Cartridge for Fendall 2000' with 7.9 gallons per cartridge and NDC code 0498-0631-37.
We’ve drafted a message you can send Honeywell to request your refund or repair — edit it as you like.
Subject: Recall D-0461-2024 — Honeywell Honeywell Hello, I own a Honeywell that is covered by recall D-0461-2024 from Honeywell. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
