Class II ยท Moderate risk
iVIZIA
Lack of Assurance of Sterility: This recall has been initiated due to CGMP deviations found by the FDA during an inspection of the manufacturer.
National Drug Code
Is NDC 82584-0700-11 recalled?
iVIZIA Dry Eye · 1 BOTTLE, DROPPER in 1 CARTON (82584-700-11) / 10 mL in 1 BOTTLE, DROPPER
Yes — this exact package was recalled
1 FDA recall names the code 82584-0700-11 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
- povidone
- Strength
- POVIDONE 25 mg/5mL
- Form
- Solution/ Drops · Ophthalmic
- Labeler
- Thea Pharma Inc.
- Type
- Human OTC Drug
- Product code
- 82584-0700
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.
Other recalled products from this labeler
- 82584-0002 Betimol 1
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