Class II · Moderate risk
Dry Eye Relief Eye Drops
Lack of Assurance of Sterility
National Drug Code
Is NDC 41250-0718-01 recalled?
Meijer Dry Eye Relief · 1 BOTTLE, DROPPER in 1 BOX (41250-718-01) / 15 mL in 1 BOTTLE, DROPPER
Yes — this exact package was recalled
2 FDA recalls name the code 41250-0718-01 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.
2 of these recalls are still ongoing.
- Active ingredient
- Glycerin, Hypromellose, Polyethylene glycol 400
- Strength
- GLYCERIN .2 g/100mL; POLYETHYLENE GLYCOL 400 1 g/100mL…
- Form
- Solution/ Drops · Ophthalmic
- Labeler
- Meijer Distribution, Inc.
- Type
- Human OTC Drug
- Product code
- 41250-0718
Recalls naming this package
Class II · Moderate risk
Dry Eye Relief Lubricant Eye Drops
CGMP Deviations: good manufacturing deficiencies related to a lack of documentation of the fill line.
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
- 41250-0852 See recall 3
- 41250-0708 See recall 2
- 41250-0989 nasal 2
- 41250-0060 See recall 1
- 41250-0106 See recall 1
- 41250-0252 See recall 1
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