FDA Medical devices recall ·
Alcon Laboratories, Inc recall
- Recall number
- Z-2108-2025
- Date
- (initiated April 28, 2025)
- Company / brand
- Alcon Research LLC
6201 South Fwy, Fort Worth, TX, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 198205
- Hazard tags
- Sterility
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Vitrectomy Procedure Pak Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' Software Version: N/A Product Description: Surgical procedure pack to interface with Alcon Constellation Surgical console. Component: N/A
Why was it recalled?
Due to the potential that some units within specific lots were damaged during the manufacturing process. The area of damage is within the same area of the lidding. While the damage in the lidding is visibly noticeable, due to risk of sterility being compromised.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot Code: Many - See 'Attachment 1 - Affected Product List' Product Description: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU Catalog Number: 8065000093 UDI-DI code: 380650000934 Lot Numbers: 177FE4 1782JM 178DEX 178TCV 179EP4 179EP3 179U0P 17AVMM 17AVMN 17AVML 17AVMP Product Description: 25+ TOTALPLUS CP PAK 20K CPM BV .9 IU Catalog Number: 8065000095 UDI-DI code: 380650000958 Lot Numbers: 1782JU 1782JT 178DF2 178TCY 178TD0 1792YF 1792YE 179U0R 17A4XT 17A4XU 17AFXT 17AVMT 17AVMU 17AVMV 17AVMW 17AVMX 17CNVC Product Description: 27+ TOTALPLUS CP PAK 20K CPM BV .9 IU Catalog Number: 8065000096 UDI-DI code: 380650000965 Lot Numbers: 1782JV 178DF4 17A4XV Product Description: TOTAL PLUS,23G,10K VALVE STD Catalog Number: 8065752435 UDI-DI code: 380657524358 Lot Numbers: 1754N7 1754NC 175M43 1762KH 176CCJ 176CCK 176WU8 176WU9 17769X 1782HM 1782HN 178T9K 179EEV 179TY3 179TY4 17A4WX 17C7FM 17C7FL Product Description: TOTAL PLUS,23GA,10K VALVE WD Catalog Number: 8065752436 UDI-DI code: 380657524365 Lot Numbers: 1762KJ 176WUA 17769Y 177FDH 1782HP 178DE8 178T9N 179EEX 179EEY 17C7FK Product Description: TOTAL PLUS,25+,10K VALVE STD Catalog Number: 8065752437 UDI-DI code: 380657524372 Lot Numbers: 1754NK 1754NL 1754NM 1754TC 1754TD 1754TE 1754TF 1754TH 175M45 175M46 175M47 175M44 1762KK 1762KL 1762KM 1762KN 176CCR 176CCL 176CCM 176CCN 176CCP 176WUD 1776A4 1776A5 1776A6 177FDJ 177FDK 177FDL 177FDM 177TUP 177TUR 177TUT 1782HU 1782HV 1782HW 178DEA 178DEC 178T9V 178T9W 178TD4 17930F 17930H 179EF3 17
Distribution
Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, and WV. The countries of Albania, Argentina, Australia, Austria, Bahamas, Bahrain, Bangladesh, Brazil, Bulgaria, Cambodia, Canada, Chile, China, Colombia, Costa Rica, Croatia, Cyprus, Ecuador, El Salvador, Finland, France, French Polynesia, Georgia, Germany, Guadeloupe, Guatemala, Hong Kong, Hungary, Iceland, India, Indonesia, Iran, Ireland, Israel, Italy, Jamaica, Japan, Kazakhstan, Kenya, Korea, Kosovo, Kuwait, Latvia, Lebanon, Luxembourg, Macao, Malaysia, Malta, Mexico, Moldova, Mongolia, Montenegro, Morocco, Netherlands, New Zealand, Oman, Pakistan, Peru, Philippines, Poland, Qatar, Republic of North Macedonia, R¿union, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovenia, South Africa, Spain, Sri Lanka, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Viet Nam.
States: Alaska Alabama Arkansas Arizona California Colorado Connecticut District of Columbia Delaware Florida Georgia Hawaii Iowa Idaho Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi Montana North Carolina Nebraska New Hampshire New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania Puerto Rico Rhode Island South Carolina South Dakota Tennessee Texas Utah Virginia Vermont Washington Wisconsin West Virginia
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2108-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.