FDA Device Intelligence
HomeDevice types › LZP

Aid, Surgical, Viscoelastic

FDA product code LZP · Class 3 · Ophthalmic

54
Registered devices
2,822
Adverse events
25
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-07-31Johnson & Johnson Surgical Vision, Inc.Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is encountered du
2019-12-03Johnson & Johnson Surgical Vision IncOphthalmic viscosurgical device may be difficult to remove from the eye, leading to increased postoperative intraocular pressure requiring additional interventi
2017-04-01Abbott Medical Optics Inc. (AMO)Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manu
2017-04-01Abbott Medical Optics Inc. (AMO)Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manu
2017-04-01Abbott Medical Optics Inc. (AMO)Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manu
2017-04-01Abbott Medical Optics Inc. (AMO)Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manu
2017-04-01Abbott Medical Optics Inc. (AMO)Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manu
2017-04-01Abbott Medical Optics Inc. (AMO)Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manu
2014-11-06Abbott Medical Optics Inc (AMO)AMO has received complaints where the finger grip dislodged while depressing the syringe plunger. The finger grip dislodgement could result in the surgeon's ha
2013-11-25C.L.R. Medicals International, Inc.CLR Medicals International Inc., initiated a nationwide recall of Viscocel and Viscocel Plus, in response to FDA inspection findings of deficiencies in the Qual

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