B Braun Medical recall: Lactated Ringer's Injection USP
B Braun Medical INC is recalling Lactated Ringer's Injection USP – 23,688 bags. The U.S. Food and Drug Administration published the recall on September 2, 2026; it began on August 12, 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 | Lactated Ringer's Injection USP |
| Brand | B Braun Medical |
| Company | B Braun Medical INC |
| Type | Drugs |
| Classification | Class I |
| Recall date | August 12, 2026 |
| Published by FDA | September 2, 2026 |
| Quantity | 23,688 bags |
| Recall ID | 99633 |
Recalled products
- Lactated Ringer's Injection USP, 1000 mL EXCEL container, Rx only, L7500, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-00
- FDA recall number
- D-0832-2026
- Codes, lots and dates
- Lot#: J4H077, Exp 30NOV2026.
- Quantity
- 23,688 bags
- Classification
- Class I
Identifiers and details
- FDA event ID
- 99633
- 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.”
Where it was sold
Nationwide. Distribution as the FDA records it: “U.S. Nationwide”
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 99633, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
Other B Braun Medical recalls
| Date | Recall | Problem | Agency |
|---|---|---|---|
| Sep 16, 2026 |  B Braun Medical recall: 0.9% Sodium Chloride InjectionDrugs · 201,472 total container | Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic mat… Most serious | FDA Class I |
| 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 |
All 3 B Braun Medical recalls →
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| Oct 7, 2026 | Apotex recall: Paroxetine Extended-Release TabletsDrugs | Failed dissolution specifications. Serious | FDA Class II |
| 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 Lactated Ringer's Injection USP recalled?
Yes. B Braun Medical INC recalled it on August 12, 2026; FDA published it September 2, 2026 (Class I). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Presence of Particulate matter.
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.