Lower riskMedical device recall · FDA · Published February 2, 2024
Beaver Visitec Irrigation Handle Recall: Missing Date Labels on Packaging
Beaver Visitec International recalls irrigation handles with missing manufacturing and expiration dates on labels. Owners should check product details and contact the company for guidance.
“Beaver Visitec Irrigation Handle Recall: Missing Date Labels on Packaging.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/56204-beaver-visitec-irrigation-handle-recall-missing-date-labels-on-packaging. Based on FDA recall #Z-1294-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1294-2024%22&limit=1).
Beaver Visitec International, Inc. recalled BVI Visitec Irrigation Handle (20/SP) units because pack and pouch labels are missing manufacturing and expiration dates, the FDA said on Feb. 2, 2024.
How to tell if you have it
Brand: Beaver Visite: International
Product: BVI Visitec Irrigation Handle (20/SP)
Catalog Number: 581012
UDI Number: 50886158002227
Lot Numbers: 21C0925, 21C0926
The hazard
The pack and pouch label is missing the manufacturing and expiration date.
Context
GovInfoNow's records show Beaver-Visitec International, Inc. has 15 other recalls on record since Nov. 3, 2017. Other recent recalls of similar products include LimFlow Vector Product Recall (Dec. 5, 2025), B Braun Discofix Four Way Stopcock Recall (Aug. 4, 2026) and Expressaire Disposable Tourniquet Cuff Recall (Aug. 24, 2026).
How to tell if you have this one
Check for the catalog number 581012 and UDI number 50886158002227 on the packaging. The lot numbers 21C0925 and 21C0926 are also associated with this recall.
Brand
Beaver Visite: International
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Labels
Look for the missing manufacturing and expiration dates on the packaging of the BVI Visitec Irrigation Handle (20/SP).
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Worldwide distribution - US Nationwide and the countries of AUSTRALIA, CANADA, GERMANY, SWITZERLAND, UNITED KINGDOM.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 47 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
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-1294-2024 (February 2, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1294-2024 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.