B. Braun Medical Lactated Ringer's Injection Recall: Particulate Matter Hazard
B. Braun Medical recalls Lactated Ringer's Injection USP 1000mL (L7500) due to particulate matter. Affected units have specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.
Recall notice
Presence of Particulate matter.
What happened, in plain English
B. Braun Medical is recalling Lactated Ringer's Injection USP 1000 mL (L7500) because it may contain particulate matter. This could cause serious health issues if the product is used as intended. Read more at govinfonow.com/recall/692848-b-braun-medical-lactated-ringer-s-injection-recall-particulate-matter.
Source Summary by GovInfoNow · govinfonow.com/recall/692848-b-braun-medical-lactated-ringer-s-injection-recall-particulate-matter · Updated September 14, 2026 · FDA enforcement record: FDA #D-0832-2026
Cite this page
“B. Braun Medical Lactated Ringer's Injection Recall: Particulate Matter Hazard.” GovInfoNow, updated September 14, 2026. https://govinfonow.com/recall/692848-b-braun-medical-lactated-ringer-s-injection-recall-particulate-matter. Based on FDA recall #D-0832-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0832-2026%22&limit=1).
Why it’s dangerous
Particulate matter in the injection can cause blockages or infections when administered into the bloodstream. This poses a risk of serious health complications for patients receiving the medication.
Who’s affected
Patients who have been prescribed this medication and are using the recalled product. Healthcare providers administering the product are also at risk if they use the recalled units.
How to tell if you have this one
Check for the product name 'Lactated Ringer's Injection USP', 1000 mL, model L7500, and lot number J4H077 with an expiration date of November 30, 2026.
- Brand
B. Braun Medical- Category
Drug
What to do — step by step
Contact Manufacturer
Reach out to B. Braun Medical for specific instructions on how to handle the recalled product.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “U.S. Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 21 days after the firm started it.
- Firm started the recall
- Published in FDA’s Enforcement Report
- FDA classified it Class I
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0832-2026 (August 12, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0832-2026 to see it in context.
- Plain-language summary written by qwen3:4b on September 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.