FDA Device Intelligence
HomeDevice types › HMX

Cannula, Ophthalmic

FDA product code HMX · Class 1 · Ophthalmic

7,303
Registered devices
801
Adverse events
28
Recalls
77
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-09-06Iantrek Inc.Potential for compromised integrity of the sterile packaging.
2024-02-02Beaver Visitec International, Inc.Pack and pouch label is missing the manufacturing and expiration date.
2022-05-25Mckesson Medical-Surgical Inc. Corporate OfficeFacility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lot
2021-04-21Anodyne SurgicalThe product may have a yellowish-brown/greenish-brown residue present at the tip of the cannula.
2021-02-25Dutch Ophthalmic USA, Inc.Mislabeled: 1281.B1D Disposable Replacement Backflush Brush Needles label states (20 gauge/0.9 mm) instead of the correct size of 23 gauge/0.6 mm and the corre
2019-12-17Vitreq BvMicroscopic tears of the sterile pouch may compromise sterility
2019-12-17Vitreq BvMicroscopic tears of the sterile pouch may compromise sterility
2019-12-17Vitreq BvMicroscopic tears of the sterile pouch may compromise sterility
2019-12-17Vitreq BvMicroscopic tears of the sterile pouch may compromise sterility
2019-12-17Vitreq BvMicroscopic tears of the sterile pouch may compromise sterility

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 docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.