Johnson & Johnson Surgical Vision, Inc. recalls

17 recalls on record · latest: March 14, 2024

Official U.S. recall history for Johnson & Johnson Surgical Vision, Inc., compiled from official government records.

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Johnson & Johnson Surgical Vision, Inc. recalls Johnson & Johnson VISION Reusable LAMINAR High Flow Irrigation Sleeve and Test Chamber 21 Gauge REF OPOHF21L The irriga…

March 14, 2024 · Medical device recalls Moderate risk Due to a manufacturing variation of the irrigation sleeves which could result i…

Johnson & Johnson Surgical Vision, Inc. recalls TECNIS Toric II OptiBlue IOL Models ZCW

December 12, 2023 · Medical device recalls Moderate risk Due to intraocular lens containing an angle out of specification (OOS). The cyl…

Johnson & Johnson Surgical Vision, Inc. recalls TECNIS Symfony, Extended Range of Vision IOL, REF: ZXR00, STERILE.EO, Rx Only

July 6, 2023 · Medical device recalls Moderate risk Their is a potential that intraocular lenses (IOLs) were manufactured with unin…

Johnson & Johnson Surgical Vision, Inc. recalls TECNIS Eyhance IOL, REF: ICB00, STERILE.EO, Rx Only

July 6, 2023 · Medical device recalls Moderate risk Their is a potential that intraocular lenses (IOLs) were manufactured with unin…

Johnson & Johnson Surgical Vision, Inc. recalls VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs (VRT-AF)

May 30, 2023 · Medical device recalls Moderate risk Weld protrusion/physical gap between the housing and pack cover, may exceed des…

Johnson & Johnson Surgical Vision, Inc. recalls FUSION Dual Pump Packs, REF: OPO73

December 7, 2022 · Medical device recalls Moderate risk Weld protrusion/physical gap between the housing and phaco pack cover, may exce…

Johnson & Johnson Surgical Vision, Inc. recalls Veritas Advanced Infusion Packs, REF: VRT-AI

December 7, 2022 · Medical device recalls Moderate risk Weld protrusion/physical gap between the housing and phaco pack cover, may exce…

Johnson & Johnson Surgical Vision, Inc. recalls Single-Use Packs, REF: OPO80

December 7, 2022 · Medical device recalls Moderate risk Weld protrusion/physical gap between the housing and phaco pack cover, may exce…

Johnson & Johnson Surgical Vision, Inc. recalls THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter, REF: D-1348-05-S. Used for catheter-based cardiac electrop…

September 7, 2022 · Medical device recalls Moderate risk Manufacturing error resulted in potential contamination of Bi-Directional navig…

Johnson & Johnson Surgical Vision, Inc. recalls Veritas Advanced Infusion Packs. Used in ophthalmic procedures.

September 1, 2022 · Medical device recalls Moderate risk As a result of returned product complaints for Veritas Phaco packs related to b…

Johnson & Johnson Surgical Vision Inc recalls TRAY RING COVER, REF OM271000, CONTAINS (1) TRAY RING COVER, STERILE R, Rx Only,

April 6, 2022 · Medical device recalls Moderate risk Potential breach in the sterility barrier for tray ring covers.

Johnson & Johnson Surgical Vision Inc recalls TECNIS Eyhance IOLs are permanent intraocular implants intended for implantation in the capsular bag. The TECNIS Simpli…

August 6, 2021 · Medical device recalls Moderate risk Nonconforming product was distributed in error. Product was nonconforming due e…

Johnson & Johnson Surgical Vision Inc recalls TECNIS Toric 1-Piece IOL, Model Number: ZCT150 +23.5D SE 1.50D CYL - Product Usage: intended to be placed in the capsul…

January 27, 2021 · Medical device recalls Moderate risk Due to the release of nonconforming Intraocular Lenses (IOLs).

Johnson & Johnson Surgical Vision Inc recalls Healon GV PRO 0.85 mL, Model (U.S.): 10-2400-14, Model (O.U.S.): 10-2705-14, 10-2715-14, 10-2725-14, and 10-2755-14

December 3, 2019 · Medical device recalls Moderate risk Ophthalmic viscosurgical device may be difficult to remove from the eye, leadin…

Johnson & Johnson Surgical Vision Inc recalls Disposable 25GA Vitrectomy Cutter, REF NGP0025, RX Only, Abbott Medical Optics Inc., The product provides the item nece…

September 24, 2018 · Medical device recalls Moderate risk Packaging error, 20GA Vitrectomy Cutter may be found in a 25GA package. Use of…

Johnson & Johnson Surgical Vision Inc recalls Abbott TECNIS 1-Piece Aspheric Acrylic IOL with the TECNIS iTEC Preloaded Delivery System, Lens Model PCB00, Sterile, R…

June 21, 2018 · Medical device recalls Moderate risk Expired intraocular lenses were distributed.

Johnson & Johnson Surgical Vision Inc recalls OptiMedica Catalys Precision Laser System, CE 0044 containing software cOS 5.00.33 Product Label for Serial Numbers: 44…

May 9, 2018 · Medical device recalls Moderate risk Software upgrade exhibits failures when executing Daily Alignment Verification…