US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 5, 2017 (9 years ago)

Sterile Eyewash (sterile isotonic phosphate buffered saline solution), 4 oz. 24 units per…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of sterility assurance: leaking containers which could lead to exposure to infectious agents.

What was recalled

Sterile Eyewash (sterile isotonic phosphate buffered saline solution), 4 oz. 24 units per box. Manufactured by Medex Cardio-Pulmonary Inc. d.b.a. Smiths Medical Company, 300 Corporate Woods Pkwy, Vernon Hills. Illinois, USA 60061. Model Number: 32-005583

Recalling firm
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0158-2018

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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