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 frequency…
Boxes labeled as Wet-Field Eraser, 18GA Blunt Tip, 45Deg., were shipped containing incorrect product a Wet-Field Eraser, 18GA Bevel Tip, Straight, Part Number: 221250
Read the official notice →- Date
- 2022-06-29
- Country
- United States
- Brand
- Beaver Visitec
- Product
- BVI Wet -Field Eraser, 18GA Blunt Tip, 45Deg.-Intended to remove tissue and control bleeding by the use of high frequency electrical…
- Classification
- Class II
- Units
- US Nationwide distribution in the states of AZ, CA, CT, DC, FL, GA, IN, MA,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2023-05-10
USBeaver Visitec International, Inc. recalls CryoTreQ- Aa disposable handheld instrument intended for ophthalmic surgery. It creates a tip at cryogenic temperatures by…
Device suddenly and forcefully disassembled after cryotherapy, potential for long-term or permanent impairment of a patient or user if a CryoTreq device suddenly or forcefully disassembles during a cryosurgery procedure.
- 2023-03-08
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Beaver Visitec International, Inc. recalls Ultracell Wick with 80cc Collection Bag, 20/box
Device packaging may contain open seals, compromising product sterility.
FDA · DeviceBeaver Visitec International, Inc.US distribution in AL, CA, CO, DC, FL, GA, IL, LA, MD, MN, MT, NC, NH, NJ, NM,…Official notice → - 2023-01-11
- US
Beaver Visitec International, Inc. recalls Beaver EdgeAhead Stiletto/MVR Knife .90mm Straight (20G)-for ocular paracentesis incisions in cataract procedures. Part…
Packaging sterile barrier has been compromised. Open seals can lead to a loss of device sterility and may lead to infection
- 2022-11-16
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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 surgery…
Incorrect configuration of the blades in the package. The blades curve to the right instead of curving to the left. If used may cause cause unintended tissue damage during the procedure or if noticed prior to use may…
FDA · DeviceBeaver Visitec International, Inc.FL, GA, IN, LA, MA, ME, VA Foreign: France, Japan, Netherlands, Switzerland,…Official notice → - 2021-12-29
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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. Part…
Kit packaging may have small holes compromising product sterility
- 2021-11-24
- US
Beaver Visitec International, Inc. recalls bvi CustomEyes Kit-Lafayette General Medical Center: CustomEyes Cataract Surgical Kits that contain Beaver Xstar Crescent…
Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees bevel-down blades contain bevel-up blades
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Other drugs & medical recalls in the United States
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Buzzagogo, LLC recalls Allergy Bee Gone for Kids Nasal Swab Remedy 0.33 FL OZ (10 mL) tubes, UPC Code 860002022116
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FDA · DrugBuzzagogo, LLCProduct was distributed via the internet to consumers, retailers and to…Official notice → - 2022-06-29
- US
CardioTek BV recalls CardioTek EP-TRACER Software V2.x.
Device did not pass electrical safety testing for adequate insulation.
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Maquet Cardiovascular, LLC recalls INTERGARD Woven Vascular Graft is a woven polyester graft coated with a bovine collagen. It has an external velour surface and…
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FDA · DeviceMaquet Cardiovascular, LLCUS Nationwide distribution in the state of SC.Official notice → - US
New Standard Device Inc recalls Metalogix Slotted 90 Tubular Wrench x 10mm REF 900104 LOT A29618A
Due to manufacturing processing error, wrench causing stripping when torqueing nuts.
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Getinge Usa Sales Inc recalls Flow-c Anesthesia System : intended for use in administering anesthesia while controlling the entire ventilation of patient Product…
Potential for crack to form on the on/off switch of the suction unit, which may result in an unreasonable risk of harm to the patient. In the worst case, the switch can break, preventing the suction unit from being…
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Olympus Corporation of the Americas recalls EVIS EXERA II Gastrointestinal Videoscope-indicated for use within the upper digestive tract (including the esophagus,…
Part (A-rubber) intended for a different model of gastrointestinal videoscope may have been used when replacing part on GIF-HQ190 during the last repair at Olympus. An Incorrect A-rubber fits tighter on the GIF-HQ190…
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