Class II · Moderate risk
Ful-Glo
Failed Impurities/Degradation Specifications: The Active Pharmaceutical Ingredient (API) used in the product is not being manufactured to the current USP monograph in regard to Unspecified Impurities.
National Drug Code
Is NDC 17478-0403 recalled?
Ful-Glo
This product was recalled — in other package sizes
No FDA recall names your exact package code, but 2 recalls cover the same product (17478-0403) in a different bottle or carton size. Worth checking with your pharmacist.
1 of these recalls is still ongoing.
This code is not in the current FDA NDC directory — usual for a product that has since been discontinued or repackaged. The details below come from the recall notices themselves.
Recalls of this product
Class III · Low risk
Fluorescein Sodium Ophthalmic Strips USP
Failed Content Uniformity Specifications: The product may not meet finished product release specifications, including the uniformity of dosage due to a packaging degradation related to the adhesive component of the paper pouch that can impact the level of fluorescein present in the strips.
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 17478-0215 See recall 3
- 17478-0283 See recall 3
- 17478-0622 See recall 3
- 17478-0711 See recall 3
- 17478-0030 See recall 2
- 17478-0062 See recall 2
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