Class II · Moderate risk
Eylea
Lack of Assurance of Sterility: Complaints of syringe breakage
National Drug Code
Is NDC 61755-0005-01 recalled?
Eylea · 1 SYRINGE, GLASS in 1 CARTON (61755-005-01) / .05 mL in 1 SYRINGE, GLASS
Yes — this exact package was recalled
2 FDA recalls name the code 61755-0005-01 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.
- Active ingredient
- aflibercept
- Strength
- AFLIBERCEPT 40 mg/mL
- Form
- Injection, Solution · Intravitreal
- Labeler
- Regeneron Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 61755-0005
Recalls naming this package
Class II · Moderate risk
Eylea
Lack of Assurance of Sterility: Complaints of syringe breakage
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
- 61755-0008 Libtayo 1
Free recall alerts
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