Recall archive / FDA company announcement
B. Braun: Lactated Ringer’s Injection, E7500, 1L — FDA announcement Apr 28, 2026
Published notice; closure not supplied
A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.
Source date Apr 28, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Lactated Ringer’s Injection, E7500, 1L
- Reason
- Products were found to contain particulate matter in solution
- Classification
- Not supplied
- Recalling firm
- B. Braun Medical Inc.
- Quantity
- Not supplied
- Agency-reported status
- Company recall announcement
- Source record identifier
- 143ec7c87165a01d
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Product Catalog Number | NDC Number | Product Description | Lot Number | Distribution Range | Expiration Date | Region Distributed; E7500 | 0264-7750-07 | LAC RNG INJ 1L E3 | J4P756 | 15NOV2024 – 06MAR2025 | 31MAY2027 | US; E7500 | 0264-7750-07 | LAC RNG INJ 1L E3 | J4S843 | 13JAN2025 – 15MAY2025 | 31MAY2027 | US |
Match all identifying details in the current notice. A brand name alone is not enough.
Product tables from the announcement
These identifying details come from the company announcement posted by FDA. Check the current notice for revisions.
| Product Catalog Number | NDC Number | Product Description | Lot Number | Distribution Range | Expiration Date | Region Distributed |
|---|---|---|---|---|---|---|
| E7500 | 0264-7750-07 | LAC RNG INJ 1L E3 | J4P756 | 15NOV2024 – 06MAR2025 | 31MAY2027 | US |
| E7500 | 0264-7750-07 | LAC RNG INJ 1L E3 | J4S843 | 13JAN2025 – 15MAY2025 | 31MAY2027 | US |
Announcement retrieved Oct 1, 2026. Official announcement.
Distribution
The product can be identified by product code E7500 or NDC 0264-7750-07. Product was distributed Nationwide to distributors, hospital, and healthcare facilities.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Fda listing date
- Apr 28, 2026
- Company announcement date
- Apr 28, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.