Why it was recalled
Lack of Assurance of Sterility; potential for fluid leakage at one of the weld sites.
Product description
Lactated Ringer's Injection USP, L 7500, 1000mL Excel Container, Rx Only, Sterile, nonpyrogenic, single dose container, B. Braun Medical Inc., Bethlehem, PA 18018, NDC 0264-7750-00.
Lot numbers, UPCs & expiration codes
Lot #: J5C802, J5C917, J5C918, Exp. 08/31/2027
Where it was sold
Nationwide in the US
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-0585-2025
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- Aug 4, 2025
- FDA report date
- Aug 20, 2025
- Quantity
- 74,088 containers
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- B BRAUN MEDICAL INC
Original FDA data
Every field from FDA enforcement report D-0585-2025, exactly as published.
Show all FDA fields
- City
- Allentown
- State
- PA
- Status
- Ongoing
- Country
- United States
- Event ID
- 97368
- Address
- 861 Marcon Blvd
- Code information
- Lot #: J5C802, J5C917, J5C918, Exp. 08/31/2027
- Postal code
- 18109-9577
- Report date
- Aug 20, 2025
- Product type
- Drugs
- Recall number
- D-0585-2025
- Classification
- Class II
- Recalling firm
- B BRAUN MEDICAL INC
- Product quantity
- 74,088 containers
- Reason for recall
- Lack of Assurance of Sterility; potential for fluid leakage at one of the weld sites.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Lactated Ringer's Injection USP, L 7500, 1000mL Excel Container, Rx Only, Sterile, nonpyrogenic, single dose container, B. Braun Medical Inc., Bethlehem, PA 18018, NDC 0264-7750-00.
- Distribution pattern
- Nationwide in the US
- Recall initiation date
- Aug 4, 2025
- Initial firm notification
- Letter
- Center classification date
- Aug 14, 2025