RecallRadar

FDA Device recall Z-1893-2019

Disposable 25GA Vitrectomy Cutter, REF NGP0025, RX Only, Abbott Medical Optics Inc., The product provides the item necessary to perform one…

On 2019-07-10 the FDA classified a Class II recall of Disposable 25GA Vitrectomy Cutter, REF NGP0025, RX Only, Abbott Medical Optics Inc., The product provides the item necessary to perform one… by Johnson And Johnson Surgical Vision, citing 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….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1893-2019
ClassificationClass II
Statusterminated
Initiated2018-09-24
Published2019-07-10
Last updated2026-09-13 11:55 UTC
CompanyJohnson And Johnson Surgical Vision
DistributionCA, MN, NC, NJ, NV, NY, OH, TX, UT, WA

Product

Disposable 25GA Vitrectomy Cutter, REF NGP0025, RX Only, Abbott Medical Optics Inc., The product provides the item necessary to perform one vitrectomy procedure. It is used to remove vitreous from the eye. It has been designed as a disposable (single use)

Reason

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 surgical technique, including corneal incision enlargement.

Identifiers

code_infoLot Number: 60084881 Mfg. date: 2017-09-05 Exp. date: 2020-09-05 UDI: (01)05050474534117 (17)200905(10)60084881

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1893-2019%22

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