Geri-Care eye drops recalled nationwide after lack of sterility assurance affects 720 bottles. The product, ARTIFICIAL TEARS with NDC 68788-7266-0, is manufactured by Preferred Pharmaceuticals, Inc. in Brooklyn, NY. The FDA recall class II points to a risk of contamination. Stop using immediately and contact a healthcare provider for guidance.
Lack of Assurance of Sterility
Consumers and healthcare providers should stop using this product immediately. Contact Preferred Pharmaceuticals, Inc. or your healthcare provider for guidance
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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.
Sterility concerns can lead to eye infections or contamination if used. IndustryPattern":["This recall is not part of a broader industry pattern."]
This recall is not part of a broader industry pattern.
Consumers may stop using the product immediately. There is a potential risk of eye infection for individuals who used affected lots.
Visit FDA enforcement page linked in recall: D-0443-2026.
Refunds or replacements guidance should be provided by Preferred Pharmaceuticals; typical recall processing timelines range 4-8 weeks.
Keep bottle, lot code, purchase receipt, and recall notice for records
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.
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.
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