Alcon Research, LLC Alcon Custom-Pak, Surgical Procedure Pack REF 14057-09, 45K W/DUOVISC CATARACT, N VIRGINIA EYE SURG CTR Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Alcon Custom-Pak, Surgical Procedure Pack REF 14057-09, 45K W/DUOVISC CATARACT, N VIRGINIA EYE SURG CTR
Brand
Alcon Research, LLC
Lot Codes / Batch Numbers
LOT # : 160NMU, UDI: (01)10380653302278
Products Sold
LOT # : 160NMU, UDI: (01)10380653302278
Alcon Research, LLC is recalling Alcon Custom-Pak, Surgical Procedure Pack REF 14057-09, 45K W/DUOVISC CATARACT, N VIRGINIA EYE SURG due to Custom surgical procedure packs contain latex gloves but are labeled as "latex free".. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Custom surgical procedure packs contain latex gloves but are labeled as "latex free".
Recommended Action
Per FDA guidance
On September 7, 2023, Alcon contacted consignees by phone to notify them of the recall. Alcon asked consignees to take the following action: 1. Discontinue using the affected lot and requested the customer confirm any quantity of remaining units in order to start the return process for any unused custom paks.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
VA
Page updated: Jan 10, 2026