Device recalls

ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number: 8065771541 Software Version: N/A Product Description: Ophthalmic Kn…

Alcon Research LLC · Alcon has detected an increase in complaint reports related to sharpness for specific ClearCut Dual Bevel Sideport and A-OK Corneal/Scleral V-Lance Ophthalmic…

Open, ClassifiedProcess controlZ-1925-2024
Open FDA's page for this record
Cfres ID
207329
Product res number
Z-1925-2024
Event date initiated
2024-04-22
Event date posted
2024-05-30
Recall status
Open, Classified
Res event number
94501
Product code
HNN
Product description
ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number: 8065771541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
Code info
Model/Catalog Number: 8065771541; UDI/DI: 00380657715411; Lot/Batch: 168NME, 168NND, 16AV17;
Firm FEI number
1610287
Recalling firm
Alcon Research LLC
Address 1
6201 aspex facility south fwy
City
Fort Worth
State
TX
Postal code
76134-2099
Additional info contact
Kristen Kellerhals 1-817-5514047
Root cause description
Process control
Product quantity
4,930 units
Reason for recall

Alcon has detected an increase in complaint reports related to sharpness for specific ClearCut Dual Bevel Sideport and A-OK Corneal/Scleral V-Lance Ophthalmic knives.

Action

On April 22, 2024 VOLUNTARY MEDICAL DEVICE FIELD CORRECTION letters to customers. Actions to be taken by the Customer / User: If a knife does not perform as expected, or if you feel it does not meet your expectation for sharpness, discontinue use of that specific knife and replace the knife with a new one to avoid potential complications. To acknowledge your receipt of this Voluntary Medical Device Correction notification, please take the following steps: 1. Forward this notification to all departments or organizations using Alcon Ophthalmic Knives. 2. Follow the risk mitigation precautions provided in this notice when using identified catalogue numbers of ophthalmic knives. 3. Please complete the attached Response Form indicating your understanding of the included instructions and return the attached Response Form via email or fax to Alcon. Email: Market.Actions@alcon.com Fax: 817-302-4337 Alcon has reported this issue to Health Authorities in accordance with applicable regulations. In the event you have experienced adverse events or product quality issues related to this communication, please contact Alcon via web (https://notifeye.alcon.com), by email (msus.safety@alcon.com) or by phone (1-800-757-9780). Adverse events or quality problems experienced with the use of this product may also be reported to the FDA MedWatch Adverse Event Reporting program either online (FDA EMAIL), by regular mail or by fax: http://www.fda.gov/Safety/MedWatch/HowToReport/default.htm. Should you have any questions or concerns about this matter or need help finding a replacement or substitute sterile standalone ophthalmic surgical knife, please call Alcon Customer Service or contact your Alcon Sales Representative.

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Austria, Belgium, Brazil, Canada, China, Columbia, Croatia, Czech Republic, Denmark, Finland, France, Germany, Greece, Hungary, India, Ireland, Italy, Japan, Korea, Kuwait, Luxembourg, Mexico, Netherlands, New Zealand, Norway, Panama, Philippines, Poland, Portugal, Puerto Rico, Romania, Singapore, Slovakia, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, Ukraine, United Arab Emirates, United Kingdom. Product distributed as sterile stand-alone knives have been placed on HOLD. Product included within Alcon Custom Pak (surgical procedure pack) are continuing to be distributed as ceasing distribution would cause immediate market shortage and result in canceled surgeries.

K numbers
K110166
Harmonized identifiers (openFDA)
Device name
Knife, Ophthalmic
Medical specialty description
Ophthalmic
Regulation number
886.4350
Device class
1
K number
K840855, K861744, K855050, K853403, K861334, K841951, K110166, K791980, K850049, K812620, K852633, K830366, K853598, K861491, K874057, K922378, K812918, K842647, K861748, K821440, K874056, K861732, K882402, K812450, K863725, K834546, K860332, K852828, K820618, K760187, K760186, K864290, K831975, K860305, K863665, K873385, K853129, K853063, K831266, K871285 +14 more
Registration number
2028632, 1058726, 3013530125, 3010687973, 9616972, 8044098, 3013938829, 9611680, 3012833022, 3015177648, 9616250, 1651405, 2523835, 9615659, 1421879, 9613083, 3003951061, 8040381, 1056350, 3002675176, 3041276591, 3005973280, 3012644327, 3002692886, 2431166, 3012494290, 3007648354, 3007589150, 1928237, 2184066, 1836161, 8031019, 3013576617, 3013497507, 9615857, 1450662, 8040278, 3017609685, 9710098, 3014680834 +169 more
FEI number
3013530125, 3010687973, 3013938829, 3015177648, 3003448211, 2523835, 3003951061, 1000140363, 1000306431, 3002675176, 3041276591, 3005973280, 3012644327, 3004216008, 3002692886, 3001180016, 3003289411, 3012494290, 3007648354, 3007589150, 1928237, 3002867000, 3002445546, 1317628, 3013576617, 3002806816, 3013497507, 1000160162, 1450662, 3000280067, 1000115048, 3012341472, 3017609685, 3000892087, 3014680834, 3009130324, 3033526648, 1045379, 3019924, 3003803182 +168 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.