Why it was recalled
Subpotent Drug
Product description
Dry Eye Test, Fluorescein Sodium, Ophthalmic Strips USP (0.12mg Fluorescein Sodium), 100 Sterile Strips (50 Pouches of 2 Strips Each), Manufactured by: Nomax, Inc, St. Louis, MO 63123, NDC: 51801-008-15
Lot numbers, UPCs & expiration codes
LOT 13336 EXP 07/23
Where it was sold
Nationwide USA
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0387-2021
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- Apr 13, 2021
- FDA report date
- May 26, 2021
- Quantity
- 78 cartons
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Nomax Inc
Original FDA data
Every field from FDA enforcement report D-0387-2021, exactly as published.
Show all FDA fields
- City
- Saint Louis
- State
- MO
- Status
- Terminated
- Country
- United States
- Event ID
- 87695
- Address
- 9735 Green Park Industrial Dr
- Code information
- LOT 13336 EXP 07/23
- Postal code
- 63123-7241
- Report date
- May 26, 2021
- Product type
- Drugs
- Recall number
- D-0387-2021
- Classification
- Class III
- Recalling firm
- Nomax Inc
- Product quantity
- 78 cartons
- Termination date
- Sep 28, 2023
- Reason for recall
- Subpotent Drug
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Dry Eye Test, Fluorescein Sodium, Ophthalmic Strips USP (0.12mg Fluorescein Sodium), 100 Sterile Strips (50 Pouches of 2 Strips Each), Manufactured by: Nomax, Inc, St. Louis, MO 63123, NDC: 51801-008-15
- Distribution pattern
- Nationwide USA
- Recall initiation date
- Apr 13, 2021
- Initial firm notification
- Letter
- Center classification date
- May 18, 2021