D-0443-2026 Class II Ongoing

Recalled by Preferred Pharmaceuticals, Inc. — Anaheim, CA

FDA drug recall D-0443-2026 was initiated by Preferred Pharmaceuticals, Inc. on Mar 25, 2026 and is designated Class II. Reason for recall: Lack of Assurance of Sterility The recall status is ongoing. Affected quantity: 720 bottles.

Recall Details

Product Type
Drugs
Report Date
Apr 15, 2026
Initiation Date
Mar 25, 2026
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
720 bottles

Product Description

Artificial Tears Lubricant Eye Drops (glycerin 0.2%, hypromellose 0.2%, polyethylene glycol 400 1%), 0.5 oz bottles, Mfg: Geri-Care; Brooklyn, New York NDC 68788-7266-0

Reason for Recall

Lack of Assurance of Sterility

Distribution Pattern

Nationwide within the United States

Code Information

Lot #: F1924R, F2024G, F2424E, G2424M, G2624P, J2424M

Source

Dataset
openFDA drug recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for D-0443-2026
openFDA file date
Nov 10, 2026
Loaded by RegDataLab
Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for D-0443-2026. Report a data issue: hello@regdatalab.com.