Beaver-Visitec International, Inc. recalls
Every recall we track for Beaver-Visitec International, Inc. — 188 in all, from 2017–2025 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Beaver-Visitec International, Inc. fell by more than half in 2025 (1, down from 162 in 2024).
All FDA recall records for Beaver-Visitec International, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 5 | 0 | 0 | 5 |
| 2018 | 0 | 1 | 0 | 1 | 2 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 1 | 9 | 0 | 10 |
| 2022 | 0 | 1 | 4 | 0 | 5 |
| 2023 | 0 | 1 | 2 | 0 | 3 |
| 2024 | 0 | 4 | 157 | 1 | 162 |
| 2025 | 0 | 0 | 1 | 0 | 1 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Beaver-Visitec International, Inc. recalls
What to do if you have a recalled Beaver-Visitec International, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Beaver-Visitec International, Inc. recalls
16 shown- Lower riskMedical device
Beaver-Visitec International, Inc. recalls BVI Leos Laser and Endoscopy System. Model Number: OME6000U.
Beaver-Visitec recalls OME6000U laser systems due to missing ferrites in USB cables, risking communication failure. Affected units have specific serial numbers and model numbers.
Beaver-VisitecDec 5, 2025 - Lower riskMedical device
Beaver Visitec International, Inc. recalls BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001113;
Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001113) due to potential low dead space causing inaccurate dosing. Affected units include specific lot numbers.
Beaver VisitecJul 26, 2024 - Lower riskMedical device
Beaver Visitec International, Inc. recalls Xstar Safety Slit Knife, 2.75 mm 45¿ Bevel Up, Model Number 378227
Beaver Visitec recalls Xstar Safety Slit Knives with incorrect blade bevel configuration. The knife may be used incorrectly due to reversed bevel orientation.
Beaver VisitecMay 10, 2024 - Lower riskMedical device
Beaver Visitec International, Inc. recalls BVI Visitec Irrigation Handle (20/SP)- Intended to be fit with a cannula for irrigation of the eye Catalog Number:
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 Visite: InternationalFeb 2, 2024 - Lower riskMedical device
Beaver Visitec International, Inc. recalls Xstar Kojo Safety Slit Knife, 2.5mm 45¿ Bevel Up, Part Number 373025
Xstar Kojo recalls 2.5mm 45-degree bevel up slit knives with part number 373025 that may have bevel down blades instead. This could cause improper cutting. Affected items were sold with lot number 6049877.
Xstar KojoOct 10, 2023 - Lower riskMedical device
Beaver Visitec International, Inc. recalls Conventional Knife Crescent 2.5mm, 55 degrees bevel up, Part Number 373807
Beaver Visitec recalls a specific lot of Conventional Crescent Knife 2.5mm with a bevel-down blade that could cause injury during use.
Beaver VisitecAug 25, 2023 - Use cautionMedical device
Beaver Visitec International, Inc. recalls CryoTreQ- Aa disposable handheld instrument intended for ophthalmic surgery. It creates a tip at cryogenic temperatures
Beaver Visitec recalls CryoTreQ-Aa disposable handheld ophthalmic surgery devices that may suddenly disassemble during cryotherapy, potentially causing permanent injury. Affected lots listed in the recall.
Beaver VisitecMar 17, 2023 - Lower riskMedical device
Beaver Visitec International, Inc. recalls Ultracell Wick with 80cc Collection Bag, 20/box
Beaver Visite: Ultracell Wick with 80cc Collection Bag (20/box) recalled due to packaging with open seals risking product contamination. Check catalog #40430 and lot numbers 21M3820/21L3403 for affected units.
Beaver VisitecDec 20, 2022 - Lower riskMedical device
Beaver Visitec International, Inc. recalls Beaver EdgeAhead Stiletto/MVR Knife .90mm Straight (20G)-for ocular paracentesis incisions in cataract procedures. Part
Beaver recalls EdgeAhead Stiletto knives with compromised sterile packaging that could lead to infection during cataract surgery. Affected units have specific part numbers and lot codes.
BeaverNov 30, 2022 - Use cautionMedical device
Beaver Visitec International, Inc. recalls Beaver Arthro-Lok Pointed Tip Curve L 4mm Blade-an orthopedic blade, which may be used in various types of orthopedic
Beaver recalls orthopedic blades that curve right instead of left, risking unintended tissue damage during surgery. Affected blades have specific catalog and lot numbers.
BeaverSep 30, 2022 - Lower riskMedical device
Beaver Visitec International, Inc. recalls BVI Wet -Field Eraser, 18GA Blunt Tip, 45Deg.-Intended to remove tissue and control bleeding by the use of high
Beaver Visitec recalls 18GA Blunt Tip Wet-Field Erasers with incorrect product shipped. Affected units have a bevel tip instead of blunt tip. No action needed as the product is safe for use.
Beaver Visite: 18GA Blunt TipApr 26, 2022 - Lower riskMedical device
Beaver Visitec International, Inc. recalls Malosa Core SMILE Pack 1-Medical Refractive Kit intended to be used to aid in cataract, corneal, or refractive surgery.
Beaver Visitec recalls Malosa Core SMILE Pack 1 kits with potential packaging holes that could compromise sterility during surgery. Affected units include specific lot numbers for cataract, corneal, and refractive surgery procedures.
Beaver VisitecNov 17, 2021 - Lower riskMedical device
Beaver Visitec International, Inc. recalls bvi CustomEyes Kit-Lafayette General Medical Center: CustomEyes Cataract Surgical Kits that contain Beaver Xstar
Beaver Visitec recalls CustomEyes cataract surgical kits containing bevel-up blades instead of bevel-down. Affected kits have specific model numbers and lot numbers.
Beaver Visite: CustomEyesOct 8, 2021 - Use cautionMedical device
Beaver-Visitec International Inc. recalls WET-FIELD OSHER THERMODOT MARKER, 25GA FINE TIP, CURVED; Part number 221270. Designed to create an ink-free, fine dot
Beaver-Visitec recalls Osher Thermodot Markers with incorrect needle tips that may cause injury during medical procedures. Affected units have specific lot numbers and part numbers.
Beaver-VisitecFeb 26, 2018 - UnratedMedical device
Beaver-Visitec International Inc. recalls Wet-Field Hemostatic Eraser Bipolar 25G, fine tip, straight, 5/SP; Part Number 221267; UDI: 30886158010549
Beaver-Visitec recalls Wet-Field Hemostatic Eraser Bipolar 25G with incorrect labeling. Affected units have Part Number 221267 and UDI 30886158010549. No remedy specified in recall notice.
Beaver-VisitecFeb 26, 2018 - Use cautionMedical device
Beaver-Visitec International Inc. recalls bvi Beaver EdgeAhead Safety Knife, (a) Sideport MVR .90mm 20G, REF 370531 (b) Sideport Angled, .60mm (23G), REF 378233
Beaver-Visitec recalls specific safety knives due to protective shield retracting, exposing the blade. Affected models include Sideport MVR .90mm 20G (REF 370531) and Sideport Angled .60mm (23G) (REF 378233).
Beaver-VisitecNov 3, 2017
Beaver-Visitec International, Inc. recall questions
How many recalls has Beaver-Visitec International, Inc. had?
188 recalls from Beaver-Visitec International, Inc. are on record with U.S. safety agencies, from 2017–2025.
What is the most recent Beaver-Visitec International, Inc. recall?
Beaver-Visitec International, Inc. recalls BVI Leos Laser and Endoscopy System. Model Number: OME6000U., dated Dec 5, 2025. Every Beaver-Visitec International, Inc. recall is listed on this page, newest first.
Why are Beaver-Visitec International, Inc. products recalled?
The most common reasons on record: Kit packaging may have small holes compromising product sterility (6); The protective shield was retracted, and the blade was exposed. (5); Device packaging may contain open seals, compromising product sterility. (2).
What should I do if I have a recalled Beaver-Visitec International, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Beaver-Visitec International, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.