Beaver-Visitec International, Inc. recalls BVI Leos Laser and Endoscopy System. Model Number: OME6000U.
Manufacturing deviation in which the ferrites specified for the USB cable assembly linking the Nurse Monitor touchscreen to the System Controller were not installed as intended. The omission of the ferrites on the USB…
Read the official notice →- Date
- 2026-01-07
- Country
- United States
- Brand
- Beaver Visitec
- Product
- BVI Leos Laser and Endoscopy System. Model Number: OME6000U.
- Classification
- Class II
- Units
- US Nationwide distribution in the states of FL, MI, OK, TX, WI.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Beaver Visitec recalls
- 2024-09-04
USBeaver Visitec International, Inc. recalls BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001113;
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in some of BVI CustomEyes Procedure…
- US
- 2024-06-26
- US
Beaver Visitec International, Inc. recalls Xstar Safety Slit Knife, 2.75 mm 45¿ Bevel Up, Model Number 378227
The wrong configuration of the blade was in the package. The bevel was on the opposite side, instead of being in front (bevel up) it was in the back (bevel down).
FDA · DeviceBeaver Visitec International, Inc.Worldwide distribution - US Nationwide and the countries of Canada, UK, and…Official notice → - 2024-03-20
- US
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: 581012
Pack and pouch label is missing the manufacturing and expiration date.
FDA · DeviceBeaver Visitec International, Inc.Worldwide distribution - US Nationwide and the countries of AUSTRALIA, CANADA,…Official notice → - 2024-01-10
- US
Beaver Visitec International, Inc. recalls Xstar Kojo Safety Slit Knife, 2.5mm 45¿ Bevel Up, Part Number 373025
One lot of Part Number 373025, Xstar¿ Kojo Safety Slit Knife 2.5mm 45¿ bevel up, incorrectly contains a bevel down blade instead of a bevel up blade.
- US
Beaver Visitec International, Inc. recalls Conventional Knife Crescent 2.5mm, 55 degrees bevel up, Part Number 373807
One lot of Conventional Crescent Knife 2.5mm, 55 degrees bevel-up contains a bevel down blade.
FDA · DeviceBeaver Visitec International, Inc.International distribution to the countries of Belgium, China, France,…Official notice →
Other drugs & medical recalls in the United States
- 2026-01-14
- US
- US
Imprimis NJOF, LLC recalls Tri-Moxi+¿ (Triamcinolone 9mg/0.6mL, Moxifloxacin 0.6 mg/ 0.6 mL) Single-Use Intraocular Injection, Imprimis NJOF, LLC., 1705 Route 46…
Presence of particulate matter - Glass like particles.
- US
Alembic Pharmaceuticals Limited recalls Fesoterodine Fumarate, Extended-release Tablets, 8 mg, 30 Tablets, Rx only, Manufactured by: Alembic Pharmaceuticals Limited,…
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
- 2026-01-07
- US
Philips Ultrasound, LLC recalls Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201, 795231, 795232,…
Retroactive: Ultrasound may experience an unexpected automatic reboot, resulting in damage to transducer.
FDA · DevicePhilips Ultrasound, LLCWorldwide - US Nationwide distribution in the states of AK, AL, AR, AZ, CA,…Official notice → - US
Sheathing Technologies Inc recalls Sheathes3D Seamless Viral Barrier, Latex-Free, 7/8"D Tapered to 2.9"W x 11.8"L (2.2cm Tapered to 7.4cm x 30cm), Non-Sterile,…
Vaginal/rectal ultrasound probe covers with a viral barrier may have product defects, which may result in contamination during use, posing an infection risk.
FDA · DeviceSheathing Technologies IncUS Nationwide distribution in the state of WA.Official notice → - US
Ferndale Laboratories, Inc. recalls Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive Model/Catalog Number: 0523-48 Product Description: Liquid…
Butyrate tube cracks during actuation, rendering product unusable.
FDA · DeviceFerndale Laboratories, Inc.Worldwide distribution - US Nationwide and the country of UK.Official notice →