Why it was recalled
Temperature abuse: Products exposed to improper temperature above drug label specifications.
Product description
Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5% (sterile), 15 mL bottle, Rx only, MFG: Bausch & Lomb, NDC 24208-730-06
Lot numbers, UPCs & expiration codes
Lot # 476261, 479751, 479741, Exp 3/31/2026
Where it was sold
Product was distributed to two medical facilities in MD and VA.
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-0661-2024
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Sep 11, 2024
- FDA report date
- Oct 2, 2024
- Quantity
- 27 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Mckesson Medical-Surgical Inc. Corporate Office
Original FDA data
Every field from FDA enforcement report D-0661-2024, exactly as published.
Show all FDA fields
- City
- Richmond
- State
- VA
- Status
- Terminated
- Country
- United States
- Event ID
- 95333
- Address
- 9954 Maryland Drive
- Address (line 2)
- Deep Run Iii Ste. 4000
- Code information
- Lot # 476261, 479751, 479741, Exp 3/31/2026
- Postal code
- 23233
- Report date
- Oct 2, 2024
- Product type
- Drugs
- Recall number
- D-0661-2024
- Classification
- Class II
- Recalling firm
- Mckesson Medical-Surgical Inc. Corporate Office
- Product quantity
- 27 bottles
- Termination date
- Jan 29, 2025
- Reason for recall
- Temperature abuse: Products exposed to improper temperature above drug label specifications.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5% (sterile), 15 mL bottle, Rx only, MFG: Bausch & Lomb, NDC 24208-730-06
- Distribution pattern
- Product was distributed to two medical facilities in MD and VA.
- Recall initiation date
- Sep 11, 2024
- Initial firm notification
- Letter
- Center classification date
- Sep 20, 2024