HONEYWELL INC: Drug Recall
Recall #D-0461-2024 · 03/29/2024
Class II: Risk
Recall Details
- Recall Number
- D-0461-2024
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- HONEYWELL INC
- Status
- Terminated
- Date Initiated
- 03/29/2024
- Location
- Charlotte, NC, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 10, 605 cartridges
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
Distribution Pattern
Nationwide USA, Canada
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.