B Braun Medical recall: 0.9% Sodium Chloride Injection
B Braun Medical INC is recalling 0.9% Sodium Chloride Injection – 201,472 total container. The U.S. Food and Drug Administration published the recall on September 16, 2026; it began on August 19, 2026. Distributed nationwide.
Most serious Class I is the most serious level: a reasonable probability that using or eating the product will cause serious health problems or death.
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| Product | 0.9% Sodium Chloride Injection |
| Brand | B Braun Medical |
| Company | B Braun Medical INC |
| Type | Drugs |
| Classification | Class I |
| Recall date | August 19, 2026 |
| Published by FDA | September 16, 2026 |
| Quantity | 201,472 total container |
| Recall ID | 99703 |
Recalled products
- 0.9% Sodium Chloride Injection, USP, 100 mL Partial Fill in 150 mL PAB Container, Sterile, Rx only, B. Braun Medical Inc., Bethlehem, PA 18018 USA, NDC 0264-1800-32.
- FDA recall number
- D-0869-2026
- Codes, lots and dates
- Lot #: J6B435, J6B444, J6B457, Exp Date: 30APR2027.
- Quantity
- 201,472 total container
- Classification
- Class I
Identifiers and details
- FDA event ID
- 99703
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Allentown, PA, United States
Why it was recalled
The reason the FDA lists: “Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyrene”
Where it was sold
Nationwide. Distribution as the FDA records it: “Nationwide within the United States”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99703, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
Other B Braun Medical recalls
| Date | Recall | Problem | Agency |
|---|---|---|---|
| Sep 9, 2026 |  B Braun Medical recall: Discofix Four Way StopcockMedical devices · 25850 | Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date print… Serious | FDA Class II |
| Sep 2, 2026 |  B Braun Medical recall: Lactated Ringer's Injection USPDrugs · 23,688 bags | Presence of Particulate matter. Most serious | FDA Class I |
All 3 B Braun Medical recalls →
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| Oct 7, 2026 | TerSera Therapeutics recall: ZoladexDrugs · 296 cartons | Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient ou… Serious | FDA Class II |
| Oct 7, 2026 | Aurolab Trust recall: FOCUS PI Hypromellose 0.7% FormulaDrugs · 25,220 bottles | a sterility problem Serious | FDA Class II |
| Oct 7, 2026 | Amneal Pharmaceuticals recall: Estradiol GelDrugs · 2,592 30-count cartons | Defective Container; packets were found to be either empty or partially full. Serious | FDA Class II |
About this recall
Is B Braun Medical 0.9% Sodium Chloride Injection recalled?
Yes. B Braun Medical INC recalled it on August 19, 2026; FDA published it September 16, 2026 (Class I). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyrene
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
Nationwide.
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.