Beaver Visitec International, Inc. recalls BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584550;
Data in RES.
Read the official notice →- Date
- 2024-09-04
- Country
- United States
- Brand
- Beaver Visitec
- Product
- BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584550;
- Classification
- Class II
- Units
- US Nationwide distribution.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2026-01-07
US
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…
FDA · DeviceBeaver-Visitec International, Inc.US Nationwide distribution in the states of FL, MI, OK, TX, WI.Official notice →- 2024-09-04
US
Beaver 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…
- 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
- 2024-09-04
US
ORTHOPEDIATRICS CANADA ULC Dba PEGA MEDICAL recalls FRT250 - 4.0-6.4 CARTRIDGE. Component of the Fassier-Duval Telescopic IM System
During the assembly of the FRT250 cartridge assembly, an incorrect component was used. Specifically, the FRT240-HEX (2) was used instead of the FRT250-HEX.
FDA · DeviceORTHOPEDIATRICS CANADA ULC Dba PEGA MEDICALWorldwide - US Nationwide distribution in the state of Texas and the countries…Official notice →US
Cypress Medical Products LLC recalls McKesson Syringe 60CC, Luer Lock Tip, Sterile, ITEM NO 102-S60C. Model No. 102-S60C - SYRINGE, LL 60CC (25/BX 4BX/CS)
Affected syringes lack FDA clearance.
FDA · DeviceCypress Medical Products LLCUS distribution only. Domestic distribution nationwide.Official notice →US
Beaver 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
MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedural kits labeled as: ARTHROGRAPH TRAY, Pack Number MNS12670A
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
US
Agfa N.V. recalls DR 800. Digital Radiography X-ray System.
Potential for the front lever chain of the DR 800 table to fail.
FDA · DeviceAgfa N.V.Worldwide - US Nationwide distribution in the states of CA, FL, IL, IN, KS,…Official notice →US
RONAN MEDICAL LLC recalls BrainFeedback Pro 2 Device - is intended as an instrument that provides a visual and auditory signal corresponding to the status of a…
Neurofeedback systems removed due to missing design and development documentation and devices may not perform as intended.
FDA · DeviceRONAN MEDICAL LLCWorldwide - US Nationwide distribution in the states of CA, FL, TN, MI, IL, CT…Official notice →