Home › Alcon Laboratories, Inc. › Alcon
Alcon
Alcon Laboratories, Inc. · Model 8065128301 · UDI-DI 00380651283015
4
510(k) clearances
895
Adverse events
4
Recalls
24
Facilities
Description
BIPOLAR CABLE 12FT THERMOPLASTIC RUBBER
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-08-05 | Alcon Research LLC | Due to incomplete seals in the pouch which provide the sterile barrier. |
| 2025-04-28 | Alcon Research LLC | 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 |
| 2018-09-24 | Johnson & Johnson Surgical Vision Inc | Packaging error, 20GA Vitrectomy Cutter may be found in a 25GA package. Use of a Vitrectomy cutter that is a different size than expected could lead to the need to alter the surgi |
| 2017-03-30 | Abbott Medical Optics Inc. (AMO) | Packaging error. 20GA Vitrectomy Cutters may be found in a 25GA package and 25GA Vitrectomy Cutters may be found in a 20GA package. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.