FDAFDA recall D-0832-2026 · Sep 2, 2026
B BRAUN MEDICAL INC: Lactated Ringer's Injection USP recall
Recall found
Product
Lactated Ringer's Injection USP, 1000 mL EXCEL container, Rx only, L7500, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-00
Reason for recall
Presence of Particulate matter.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class I: FDA's most serious class, where use of or exposure to the product may cause serious health problems or death.
- Status
- Ongoing
- Codes, lots and dates
- Lot#: J4H077, Exp 30NOV2026.
- Quantity
- 23,688 bags
- Distribution
- U.S. Nationwide
- Recalling firm
- B BRAUN MEDICAL INC, Allentown, PA
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-08-12
Source: openFDA enforcement record D-0832-2026 · search recall number D-0832-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.