Quick Facts at a Glance
- Recall Date
- March 25, 2026
- Hazard Level
- HIGH
- Brands
- ARTIFICIAL TEARS, Preferred Pharmaceuticals Inc.
- Category
- Health & Personal Care
- Sold At
- Unknown
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL, PREGNANT, PREGNANT
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- ARTIFICIAL TEARS, Preferred Pharmaceuticals Inc.
- Product type
- Eye Drops
- Model numbers
- Lot #: F1924R, F2024G, F2424E, G2424M, G2624P, J2424M
- UPC codes
- 68788-7266, 68788-7266-0
- Sizes
- 0.5 oz
- Sold at
- Unknown
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
March 25, 2026
Reported by FDA DRUG
April 15, 2026
RecallRadar source check
April 22, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Lack of Assurance of Sterility
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact Preferred Pharmaceuticals, Inc. or your healthcare provider for guidance
About This Product
Artificial Tears Eye Drops are lubricating eye drops designed to relieve dryness and irritation. They are used to moisten the eye and supplement tear film in dry eye conditions.
Why This Is Dangerous
Sterility concerns can lead to eye infections or contamination if used. IndustryPattern":["This recall is not part of a broader industry pattern."]
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers may stop using the product immediately. There is a potential risk of eye infection for individuals who used affected lots.
Practical Guidance
How to identify if yours is affected
- Check NDC 68788-7266-0 on bottle label.
- Check Lot numbers: F1924R, F2024G, F2424E, G2424M, G2624P, J2424M.
- 0.5 oz bottle appearance.
Where to find product info
Visit FDA enforcement page linked in recall: D-0443-2026.
What timeline to expect
Refunds or replacements guidance should be provided by Preferred Pharmaceuticals; typical recall processing timelines range 4-8 weeks.
If the manufacturer is unresponsive
- File a complaint with FDA MedWatch if company delays
- Keep records of all correspondence and receipts
- Consider contacting consumer protection agencies
How to prevent similar issues
- In the future, verify sterility controls during manufacturing
- Check for FDA recall notices on official agency portals
- Avoid buying unlabeled or questionable lots
Documentation advice
Keep bottle, lot code, purchase receipt, and recall notice for records
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Product Details
Product: Artificial Tears Lubricant Eye Drops. Size: 0.5 oz bottles. Manufacturer: Geri-Care. Location: Brooklyn, New York. NDC: 68788-7266-0. Quantity recalled: 720 bottles. Distribution: Nationwide in the United States. Brand: ARTIFICIAL TEARS.
Reported Incidents
No specific injuries or incidents are cited in the provided information. If none are reported, the section would state: No injuries or incidents have been reported.
Key Facts
- High hazard level
- Active recall as of 2026-03-25
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Safety Guide
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