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Lower risk Medical device recall · FDA · Published August 25, 2023

Beaver Visitec Conventional Knife Recall: Bevel Down Blade Hazard

Beaver Visitec recalls a specific lot of Conventional Crescent Knife 2.5mm with a bevel-down blade that could cause injury during use.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0632-2024Medical deviceBeaver Visitec ›
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Contact the company

Recalling firmBeaver Visitec International, Inc.500 Totten Pond Rd, 10 City Point · Waltham, MA 02451-1916
✎ GovInfoNow plain-language explainer

Beaver Visitec is recalling a specific lot of Conventional Crescent Knife 2.5mm with a bevel-down blade. This defect could cause injury if the knife is used as intended. Read more at govinfonow.com/recall/57441-beaver-visitec-conventional-knife-recall-bevel-down-blade-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/57441-beaver-visitec-conventional-knife-recall-bevel-down-blade-hazard · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0632-2024

Cite this page

“Beaver Visitec Conventional Knife Recall: Bevel Down Blade Hazard.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/57441-beaver-visitec-conventional-knife-recall-bevel-down-blade-hazard. Based on FDA recall #Z-0632-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0632-2024%22&limit=1).

Beaver Visitec International, Inc. recalled Conventional Knife Crescent 2.5mm with part number 373807 due to a bevel-down blade hazard, according to the FDA on 2023-08-25.

How to tell if you have it

  • Brand: Beaver Visitec
  • Product: Conventional Knife Crescent 2.5mm, 55 degrees bevel up
  • Part Number: 373807
  • UDI-DI: 30886158000571
  • Lot Number: 6054027
  • Quantity: 1980 units

The hazard

One lot of the Conventional Crescent Knife contains a bevel down blade instead of the intended bevel up configuration.

Context

GovInfoNow's records show Beaver-Visitec International, Inc. has 15 other recalls on record since 2017-11-03. Other recent recalls of similar products include D.O.R.C. TDC VELOCE 23G Cutter Recall (2026-04-30), D.O.R.C. TDC VELOCE 27G Cutter Recall (2026-04-30) and D.O.R.C. TDC VELOCE 25G Cutter Recall (2026-04-30).

How to tell if you have this one

Check for the part number 373807 and lot number 6054027 on the knife. The UDI-DI code 30886158000571 is also associated with this specific lot.

  • Brand
    Beaver Visitec
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the part number 373807 and lot number 6054027 on the knife to confirm if it is recalled.

How this recall unfolded

Recall timeline

FDA published this recall 5 months after the firm started it.

1. Firm started the recall: Aug 25, 202312. FDA classified it Class II: Jan 4, 202423. Published in FDA’s Enforcement Report: Jan 10, 2024320232024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

What should I do if I have this knife?

Check the product details to see if it matches the recalled lot. If it does, you may want to contact the manufacturer for further instructions.

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Where this comes from

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-0632-2024 (August 25, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0632-2024 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA