B. Braun Medical Inc. Issues Voluntary North American Recall of Excel® Lactated Ringers Injection, 1000mL Due to the Presence of Particulate Matter
Summary & scoring by The Bell Brief (Dr. Jennifer Bell) using the Drill-Down Protocol (Drill-Down Score) — not the original publisher.
Why it matters for dental
Dental practices and oral surgery centers that stock IV fluids for sedation or emergency protocols must immediately quarantine and replace the recalled lot of B. Braun Excel® Lactated Ringers Injection to avoid infusing particulate matter, which could trigger adverse events during procedures.
Key points
- Recall date: August 19, 2026; lots distributed to hospitals, clinics, and dental surgery centers.
- Product: 0.9% Sodium Chloride Injection USP, 100 mL in 150 mL PAB® containers; three lots recalled due to visible particulate matter.
- Action required: Stop use, quarantine stock, and follow B. Braun’s return instructions to avoid liability or patient harm.
- Dental risk: Particulates introduced during implant placement, extractions, or IV sedation can lead to foreign-body granulomas, bacteremia, or compromised healing.
Who should care
Original reporting · 4 sources
This brief consolidates coverage from multiple outlets. Open any source for full reporting and paywalled content — we summarize and score; we do not republish.
- Open originalFDA RecallsPrimary
B. Braun Medical Inc. Issues Voluntary North American Recall of Excel® Lactated Ringers Injection, 1000mL Due to the Presence of Particulate Matter · fda.gov
- Open originalFDA Recalls
B. Braun Medical Inc. Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container Due to the Presence of Particulate Matter · fda.gov
- Open originalFDA Recalls
Baxter Issues Voluntary Nationwide Recall for One Lot of 70% Dextrose Injection Due to Potential Presence of Particulate Matter · fda.gov
- Open originalFDA Recalls
Baxter Issues Voluntary Nationwide Recall for Two Lots of 0.9% Sodium Chloride Injection Due to Potential Presence of Particulate Matter · fda.gov
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