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.
Labeling: Not Elsewhere Classified - the description, warnings, storage information and instructions for use are either missing or partially printed.
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.
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.
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.
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.
Verify that the label has all required information including warnings, storage instructions, and usage details.
The recall indicates missing or partially printed labels, which could lead to incorrect use. It is not safe to use without complete labeling.
The recall does not specify a remedy, so check the label for completeness and contact your healthcare provider for guidance.
Look for the product name '0.9% Sodium Chloride Injection USP, 1000 mL Excel Plus Container' with lot number 0061852531 and expiration date 2/28/2025.
We’ve drafted a message you can send B. Braun Medical to request your refund or repair — edit it as you like.
Subject: Recall D-1083-2023 — B. Braun Medical B. Braun Medical Hello, I own a B. Braun Medical that is covered by recall D-1083-2023 from B. Braun Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
