← FDA ENFORCEMENT
D-0461-2024Class II

HONEYWELL INC

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
HONEYWELL INC
Product type
Drug
Status
Terminated
Report date
2024-05-01
Distribution
Nationwide USA, Canada
Firm state
NC
Product quantity
10, 605 cartridges
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Risk Management & CAPA
Reason for recall

CGMP Deviations

Product description

Eyesaline, Saline Eyewash Solution, Cartridge for Fendall 2000, Net contents: 7.9 gal per cartridge, Sperian Eye & Face Protection, Inc., 825 East Highway 151, Platteville, WI 53818. NDC: 0498-0631-37

Code / lot info

Manufacturer's Product Number/ Catalog Number: 32-002050-0000; Exp 06/21/2025

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →