FDA recall, , High risk
B. Braun Lactated Ringer's Injection
Lactated Ringer's Injection may contain particulate matter that can cause patient harm.
Summary by Recall Canary from the FDA notice
What happened
B. Braun Medical Inc., of Allentown, Pennsylvania, recalled 95,412 containers of Lactated Ringer's Injection USP, 1000 mL, Rx only, because the products were found to contain particulate matter in solution. The recall began on April 28, 2026, and was added to the FDA's Enforcement Report on May 6, 2026, with classification on May 18, 2026.
The product is distributed nationwide in the U.S.A. The recalled containers are from B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA.
What to do
If a code on your package is listed below:
- Consumers and distributors that have product which is being recalled should stop using and arrange for return of the product using the Urgent Pharmaceutical Recall Acknowledgement form provided by the company.
- Consumers with questions regarding this recall can contact B. Braun’s Recalls Department at 844-903-6417 or recalls@
bbraunusa.com, Monday to Friday from 8:00 am to 5:00 pm 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 yours affected?
Match the NDC and lot code listed under your product.
An NDC (National Drug Code) is usually printed on the drug's label.
Lactated Ringer's Injection USP
- NDC
- 0264-7750-07
- Lot code
- J4P756
- J4S843
Recall details
- Company began the recall
- Sold in
U.S.A. 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
- 98795
- Recall number
- D-0540-2026
- Quantity recalled
- 95,412 containers
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
Added to FDA's Enforcement Report
Listed on Recall Canary
In FDA's weekly enforcement report
Classified by FDA
Summary updated
