Class II · Moderate risk
CHNaO Fluorescein Sodium Ophthalmic Strips
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
National Drug Code
Is NDC 83851-0100-30 recalled?
C20H10Na2O5 Fluorescein Sodium Ophthalmic Strips · 300 PACKET in 1 BOX (83851-100-30) / 1 mg in 1 PACKET
Yes — this exact package was recalled
1 FDA recall names the code 83851-0100-30 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Fluorescein Sodium
- Strength
- FLUORESCEIN SODIUM 1 mg/mg
- Form
- Strip · Ophthalmic
- Labeler
- Vistamerica USA
- Type
- Human Prescription Drug
- Product code
- 83851-0100
Recalls naming this package
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.
Free recall alerts
Know the day your medication is recalled
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