B. Braun Medical Recalls 1000mL Sodium Chloride Injection Due to Missing Labels
B. Braun Medical recalls 1000mL 0.9% Sodium Chloride Injection USP Excel Plus containers with missing or incomplete labeling. This affects prescription-only products sold with specific lot numbers.
Lower-risk recall
Labeling: Not Elsewhere Classified - the description, warnings, storage information and instructions for use are either missing or partially printed.
Contact the company
What happened, in plain English
B. Braun Medical is recalling 1000mL 0.9% Sodium Chloride Injection USP Excel Plus containers because the labels are missing or partially printed. This could lead to incorrect use or storage, especially since the product is prescription-only. Read more at govinfonow.com/recall/33229-b-braun-medical-recalls-1000ml-sodium-chloride-injection-due-to.
Source Summary by GovInfoNow · govinfonow.com/recall/33229-b-braun-medical-recalls-1000ml-sodium-chloride-injection-due-to · Updated August 17, 2026 · FDA enforcement record: FDA #D-1083-2023
Cite this page
“B. Braun Medical Recalls 1000mL Sodium Chloride Injection Due to Missing Labels.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/33229-b-braun-medical-recalls-1000ml-sodium-chloride-injection-due-to. Based on FDA recall #D-1083-2023 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1083-2023%22&limit=1).
Why it’s dangerous
The product's labeling is missing or partially printed, which could lead to incorrect storage, dosage errors, or improper use. Since this is a prescription medication used in medical settings, incomplete labeling might cause safety issues if not addressed.
Who’s affected
Prescription patients who received this specific container. Healthcare providers using the product for medical treatments may be at higher risk due to the critical nature of the medication.
How to tell if you have this one
Check for the product name '0.9% Sodium Chloride Injection USP, 1000 mL Excel Plus Container' with the lot number 0061852531 and expiration date 2/28/2025. This product is only available by prescription.
- Brand
B. Braun Medical- Category
Drug
What to do — step by step
Check Label Completeness
Verify that the label has all required information including warnings, storage instructions, and usage details.
How this recall unfolded
Recall timeline
FDA terminated this recall 23 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
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-1083-2023 (August 2, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1083-2023 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 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.