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Alcon Research LLC Aspex Facility

Alcon Research LLC Aspex Facility Recalls

All product recalls associated with Alcon Research LLC Aspex Facility.

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Recall Summary

Total Recalls

1000

Past Year

53

Class I (Serious)

166

Most Recent

Dec 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 81–100 of 1369 recalls

25+ Total Plus Pak (Alcon) – Sharpness Complaint (2024)

Laceration Risk

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

FDAJul 15, 2024Nationwide• Alcon Research LLC Aspex Facility

Total Plus Valve (Alcon) – Sharpness Complaint (2024)

Laceration Risk

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

FDAJul 15, 2024Nationwide• Alcon Research LLC Aspex Facility

25+ CMB Pak (Alcon) – Sharpness Complaint (2024)

Laceration Risk

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

FDAJul 15, 2024Nationwide• Alcon Research LLC Aspex Facility

20 Gauge V-Lance Knife (Alcon) – Sharpness Complaint (2024)

Laceration Risk

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

FDAJul 15, 2024Nationwide• Alcon Research LLC Aspex Facility

ClearCut Sideport Knife (Alcon) – Sharpness Complaint (2024)

Laceration Risk

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

FDAJul 15, 2024Nationwide• Alcon Research LLC Aspex Facility

Total Plus Valve (Alcon) – Sharpness Complaint (2024)

Laceration Risk

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

FDAJul 15, 2024Nationwide• Alcon Research LLC Aspex Facility

25+ Total Plus Pak (Alcon) – Sharpness Complaint (2024)

Laceration Risk

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

FDAJul 15, 2024Nationwide• Alcon Research LLC Aspex Facility

Product Name: ClearCut S Safety Sideport Knife 1.0mm Dual... (Alcon Research LLC Aspex Facility) – laceration hazard (2024)

Laceration Risk

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

FDAJul 15, 2024Nationwide• Alcon Research LLC Aspex Facility

Product Name: 25+ TTL PLUS VPAK 20000CPM BWV Model/Catalo... (Alcon Research LLC Aspex Facility) – laceration hazard (2024)

Laceration Risk

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

FDAJul 15, 2024Nationwide• Alcon Research LLC Aspex Facility

Alcon Custom Pak (Alcon) – Sharpness Complaint (2024)

Laceration Risk

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

FDAJul 15, 2024Nationwide• Alcon Research LLC Aspex Facility

5 Lead Cable System (Stryker) – Packaging Mixup (2024)

Disposable 5 lead cable and lead wire system package that should contain lead systems, lead telemetry systems and a dual connect cable, may in fact contain, different ECG Leads, which are not approved for reprocessing, but that may have been reprocessed, which may lead to devices not performing as intended.

FDAJul 2, 2024Nationwide• Stryker Sustainability Solutions

Zimmer Tourniquet Cuff (Stryker) – Mislabeling Issue (2024)

Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.

FDAMay 31, 2024Nationwide• Stryker Sustainability Solutions

VICINITY VI33 (VICINITY) – CNG System Leak (2024)

Vicinity Motor Corporation (Vicinity) is recalling certain 2017 Vi33 and 2022 Vi35 buses powered by compressed natural gas (CNG). The low-pressure CNG hoses and fittings are insufficient and may leak. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 304, "Compressed Natural Gas Fuel Container Integrity."

NHTSAMay 30, 2024Nationwide• VICINITY

Colby Jack Cheese Slices (Tillamook) – plastic material (2024)

Plastic material. The piece of plastic material was detected in a 40lb. cheese block and smaller fragments of the plastic material may be found in the cheese slices.

Class IIModerate

FDAMay 30, 2024IN, UT, WA• Tillamook County Creamery Association

Suntegrity Sunscreen (Synchronicity) – CGMP Deviations (2024)

CGMP Deviations

Class IIModerate

FDAMay 24, 2024Nationwide• SYNCHRONICITY SPA INC, DBA SUNTE

Suntegrity Sunscreen (Synchronicity) – Microbial Contamination (2024)

Microbial Contamination of Non-Sterile Products: Presence of Aspergillus Sydowii (Mold)

FDAMay 24, 2024Nationwide• SYNCHRONICITY SPA INC, DBA SUNTE

Surgical Image Guidance (Alcon) – Software Movement Error (2024)

After surgery initiation, while using surgical image guidance, if significant eye rotation/movement occurs, a software anomaly may cause re-establishment of incorrect new registration angle, range indicator will display incorrectly, which could result in incorrect placement of toric IOL axis, which could cause astigmatic error under/over correction resulting in decreased uncorrected visual acuity.

FDAMay 23, 2024Nationwide• Alcon Research LLC Aspex Facility

BRAUNABILITY CHRYSLER WHEELCHAIR VAN (BRAUNABILITY) – Seat Mechanism Issue (2024)

The Braun Corporation (Braun) is recalling certain 2023-2024 Chrysler Voyager vehicles, equipped with certain GO-ES Space Saver Foldaway Seats. The recliner mechanism may not engage when the seat back is fully reclined. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 210, "Seat Belt Assembly Anchorages."

NHTSAMay 17, 2024Nationwide• BRAUNABILITY

Crab Cake (County Road Seafood) – Undeclared Egg (2024)

Undeclared Allergen

Product contains (allergen) undeclared egg.

FDAMay 15, 2024NC, SC• County Road Seafood, LLC

BW Lasso Diagnostic EP Catheter (Stryker) – Testing Requirements (2024)

Diagnostic electrophysiology (EP) catheters do not meet testing requirements.

FDAMay 10, 2024Nationwide• Stryker Sustainability Solutions