FDA action counts
| Total FDA actions | 22 |
|---|---|
| Warning letters | 0 |
| Recalls | 22 |
| Approval records | 0 |
| Form 483 inspection citations | 0 |
| Most recent action | June 10, 2026 |
Enforcement history
On 2026-04-22, Argus HQ recorded a FDA recall for B BRAUN MEDICAL INC, rated "critical" severity in Argus HQ's classification: B Braun Medical Inc — Class I recall: B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG DR. Mode… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-04-22, Argus HQ recorded a FDA recall for B BRAUN MEDICAL INC, rated "critical" severity in Argus HQ's classification: B Braun Medical Inc — Class I recall: B Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 4.8MM PUMP SEGMENT. Model N… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-04-22, Argus HQ recorded a FDA recall for B BRAUN MEDICAL INC, rated "critical" severity in Argus HQ's classification: B Braun Medical Inc — Class I recall: B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG. Model Num… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-04-22, Argus HQ recorded a FDA recall for B BRAUN MEDICAL INC, rated "critical" severity in Argus HQ's classification: B Braun Medical Inc — Class I recall: B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC. Model… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-04-22, Argus HQ recorded a FDA recall for B BRAUN MEDICAL INC, rated "critical" severity in Argus HQ's classification: B Braun Medical Inc — Class I recall: B. Braun Hemodialysis Bloodlines, STREAMLINE FRESENIUS FOR DAVITA. Model Number:… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-04-22, Argus HQ recorded a FDA recall for B BRAUN MEDICAL INC, rated "critical" severity in Argus HQ's classification: B Braun Medical Inc — Class I recall: B. Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 2.6MM PUMP SEGMENT. Model… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-04-29, Argus HQ recorded a FDA recall for B BRAUN MEDICAL INC, rated "high" severity in Argus HQ's classification: B BRAUN MEDICAL INC — Class II recall: DEXTROSE INJECTION USP, 70%, 2000 mL bags, Rx only, Sterile, B. Braun Medical In… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-04-29, Argus HQ recorded a FDA recall for B BRAUN MEDICAL INC, rated "high" severity in Argus HQ's classification: B BRAUN MEDICAL INC — Class II recall: 0.9 % SODIUM CHLORIDE IRRIGATION, USP, 3000 mL bags, Rx only, Sterile, B. Braun… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-04-29, Argus HQ recorded a FDA recall for B BRAUN MEDICAL INC, rated "high" severity in Argus HQ's classification: B BRAUN MEDICAL INC — Class II recall: LACTATED RINGER'S IRRIGATION, 3000 mL bags, Sterile, Ex only, B. Braun Medical I… An FDA recall record.
Risk pattern analysis
Argus HQ analysis — not an FDA finding
This section is Argus HQ analysis, not an FDA finding. B BRAUN MEDICAL INC has 22 separate FDA recalls on file, more than a single isolated recall event. A pattern across multiple FDA touchpoints does not by itself establish that any specific product currently poses a risk; it reflects only the frequency of FDA engagement with this company as recorded in Argus HQ's database. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed.
Frequently asked questions
- What is the most recent FDA action on file for B BRAUN MEDICAL INC?
- June 10, 2026. Argus HQ ingests new FDA enforcement records daily.
- Has B BRAUN MEDICAL INC had product recalls?
- Yes, 22 recalls on file. See the full history below for each one.
- Is this FDA enforcement data for B BRAUN MEDICAL INC official?
- Every record links directly to its primary FDA.gov source. Argus HQ aggregates and structures public FDA data; the verbatim FDA record is always the source of truth.
- How many FDA actions has B BRAUN MEDICAL INC had?
- Argus HQ has recorded 22 FDA events for B BRAUN MEDICAL INC: 0 warning letters, 22 recalls, 0 approvals, and 0 Form 483 inspection observations. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.
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Related enforcement actions
- B Braun Medical Inc — Class II recall: Brand Name: B. BRAUN MEDICAL INC. Product Name: SESK UPMC DOUBLE CATHETER TRAY… →
- B Braun Medical Inc — Class II recall: Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK RIVERSIDE HEALTH SYSTEM M… →
- B Braun Medical Inc — Class I recall: Spinal Needle procedure kits: Material Description (Material Number) 24GA. PE… →
- B Braun Medical Inc — Class II recall: Brand Name: B. BRAUN MEDICAL INC. Product Name: BPSK, BLOCKJOCKS TRAY Model/Ca… →
- B Braun Medical Inc — Class II recall: Brand Name: B. BRAUN MEDICAL INC. Product Name: NES1725KFXL SPINAL EPID CLOSED… →
- B Braun Medical Inc — Class I recall: Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material D… →
- B Braun Medical Inc — Class II recall: Brand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY… →
- B Braun Medical Inc — Class II recall: Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK HARRIS METHODIST Model/Ca… →
- B Braun Medical Inc — Class II recall: Brand Name: B. BRAUN MEDICAL INC. Product Name: LYNDON B JOHNSON HOSPITAL SPINA… →
- B Braun Medical Inc — Class II recall: Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK SHANDS JACKSONVILLE 200557… →
Compare with
Two different companies merged onto this page by mistake? Or a name variant missing? Tell us — corrections@argushq.ai
Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder
Cite this record
Reusing this data in reporting or research? Here’s a ready-made citation.
Argus HQ Research (2026). B BRAUN MEDICAL INC's Complete FDA Record. Digital Empire LLC. Retrieved from https://argushq.ai/company/b-braun-medical-inc
"B BRAUN MEDICAL INC's Complete FDA Record." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/company/b-braun-medical-inc.
Argus HQ Research. "B BRAUN MEDICAL INC's Complete FDA Record." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/company/b-braun-medical-inc.
@misc{argushq_argushq_ai_company_b_braun_medical_inc_2026,
title = {B BRAUN MEDICAL INC's Complete FDA Record},
author = {{Argus HQ Research}},
year = {2026},
publisher = {Digital Empire LLC},
url = {https://argushq.ai/company/b-braun-medical-inc},
note = {Accessed: July 13, 2026}
}Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗

