Recall Z-1956-2025— Contamac Solutions, Inc.

Name: FDA recall Z-1956-2025
Creator: U.S. Food and Drug Administration
Published: 2025-05-15

Class II · Ongoing

Class II FDA medical device recall by Contamac Solutions, Inc., initiated 2025-05-15. It names one FDA 510(k) clearance: K181566. Product: Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution. Reason: Contact lens insertion solution may lack sterility..

Recalling firm: Contamac Solutions, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2025-05-15
Firm location: Grand Junction, CO, United States

510(k) clearances named in this recall

1 on FDA's record

K181566 — NutrifillContamac, Ltd.·cleared 2018-10-22

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution

Reason for recall

Contact lens insertion solution may lack sterility.

Data sourced from openFDA. This site is unofficial and independent of the FDA.