Lower riskMedical device recall · FDA · Published March 15, 2021
B. Braun Filtered Triple-Leg Extension Set Recall: Potential occlusion risk
B. Braun recalls Filtered Triple-Leg Extension Set (catalog 477034) due to potential occlusion or inability to prime. Affected lots: 00SL713784, 0061741483, 0061755034, 0061755296.
“B. Braun Filtered Triple-Leg Extension Set Recall: Potential occlusion risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/63097-b-braun-filtered-triple-leg-extension-set-recall-potential-occlusion. Based on FDA recall #Z-1509-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1509-2021%22&limit=1).
B. Braun Medical, Inc. recalled Filtered Triple-Leg Extension Sets on March 15, 2021, due to potential occlusion or priming failure, the FDA announced. The company initiated this voluntary Class II recall affecting 1,900 units distributed in North Carolina and California.
How to tell if you have it
Brand: B. Braun
Product: Filtered Triple-Leg Extension Set - Intravascular administration set
Catalog Number: 477034
Lot Codes: 00SL713784, 0061741483, 0061755034, 0061755296
The hazard
B. Braun Medical identified through complaints that the extension set may become occluded or unable to prime. The product is a sterile, single-use intravascular direct injection, intermittent infusion, continuous infusion or aspiration of fluids and medications.
Context
GovInfoNow's records show B BRAUN MEDICAL INC has 66 other recalls on record since October 15, 2013. Recent recalls include a 2026-08-19 recall for particulate matter in Sodium Chloride Injection and a 2026-08-12 recall for particulate matter in Lactated Ringer's Injection. Other recent recalls of similar products include BD 60-In Extension Sets (June 16, 2026) and Medline Kits with B. Braun IV Sets (November 26, 2025).
How to tell if you have this one
Check for the product catalog number 477034 on the packaging. Affected lots include 00SL713784, 0061741483, 0061755034, and 0061755296.
Brand
B. Braun
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Lot Number
Look for the lot numbers 00SL713784, 0061741483, 0061755034, or 0061755296 on the packaging.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 2 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of NC, CA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, North Carolina.
Recall timeline
FDA terminated this recall 15 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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 #Z-1509-2021 (March 15, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1509-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.