FDA recall, , High risk
B. Braun Lactated Ringer's Injection
Presence of Particulate matter.
Summary by Recall Canary from the FDA notice
What happened
B. Braun Medical Inc., of Allentown, Pennsylvania, began a recall of Lactated Ringer's Injection USP, 1000 mL EXCEL container, Rx only, L7500, on August 12, 2026, and announced it on August 19, 2026, due to the presence of particulate matter. The particulate matter was identified primarily as cellulose cotton fibers, with individual particles also identified as cellulose wood fiber and polystyrene. The product was distributed nationwide.
The FDA added the recall to its Enforcement Report on August 24, 2026, and it was in the weekly enforcement report on September 2, 2026, with classification on September 3, 2026.
What to do
If a code on your package is listed below:
- Customers that have the recalled product should return to place of purchase.
- Consumers with questions regarding this recall can contact B. Braun by emailing recalls@
bbraunusa.com, Monday to Friday 8:00am to 5:00pm EST. - Contact your physician or healthcare provider if you have experienced any problems that may be related to taking or using this drug product.
Is your container affected?
Match the lot code, best-by or expiration date and NDC listed under your product.
An NDC (National Drug Code) is usually printed on the drug's label.
B. Braun Excel® Container Lactated Ringers Injection, 1000ml
- NDC
- 0264-7750-00
- Lot code
- J4H077
- Best-by or expiration date
- 30NOV2026
Recall details
- Company began the recall
- Sold in
U.S. Nationwide
- Company
- B Braun Medical IncAllentown, Pennsylvania
- Hazard
- Foreign object
- Risk
High risk
There is a reasonable chance that taking it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- Event ID
- 99633
- Recall number
- D-0832-2026
- Quantity recalled
- 23,688 bags
All recalls from B Braun Medical Inc
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Announced by the company · Listed on Recall Canary
Added to FDA's Enforcement Report
In FDA's weekly enforcement report
Classified by FDA
Summary updated
