Abbott Medical Optics Inc. (AMO) recalls

Abbott Medical Optics Inc. (AMO) has 19 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 24 May 2017. The most frequent reason is labeling errors.

Total recalls19since 2013
Last 12 months0reported
Class I00% of total
Ongoing0latest 24 May 2017

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 19 100%Class III 0 0%

Why abbott medical optics inc. (amo) is recalled

By year

All abbott medical optics inc. (amo) recalls, newest first

19 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIAMO Vitrectomy Cutter recalled by Abbott Medical Optics Inc.Abbott Medical Optics Inc. (AMO)Packaging DefectsAZ
DeviceCLASS IIHealon V recalled by Abbott Medical Optics Inc.Abbott Medical Optics Inc. (AMO)Particulate MatterCA
DeviceCLASS IIHealon Duet recalled by Abbott Medical Optics Inc.Abbott Medical Optics Inc. (AMO)Particulate MatterCA
DeviceCLASS IIHealon, Part No. 10290953, 10295210 recalledAbbott Medical Optics Inc. (AMO)Particulate MatterCA
DeviceCLASS IIHealon 5 Pro recalled by Abbott Medical Optics Inc.Abbott Medical Optics Inc. (AMO)Particulate MatterCA
DeviceCLASS IIHealon Pro recalled by Abbott Medical Optics Inc.Abbott Medical Optics Inc. (AMO)Particulate MatterCA
DeviceCLASS IIHealon GV recalled by Abbott Medical Optics Inc.Abbott Medical Optics Inc. (AMO)Particulate MatterCA
DeviceCLASS IIAMO Tecnis CL Foldable Silicone IOL with OptiEdge Design recalledAbbott Medical Optics Inc. (AMO)Labeling ErrorsNationwide
DeviceCLASS IITecnis Multifocal 1-Piece Intraocular Lens recalledAbbott Medical Optics Inc. (AMO)Labeling ErrorsNationwide
DeviceCLASS IITecnis 1-Piece IOL recalled by Abbott Medical Optics Inc.Abbott Medical Optics Inc. (AMO)Labeling ErrorsNationwide
DeviceCLASS IITecnis OptiBlue 1-Piece Iol recalled by Abbott Medical Optics Inc.Abbott Medical Optics Inc. (AMO)Labeling ErrorsNationwide
DeviceCLASS IITecnis Multifocal Foldable Acrylic Intraocular Lens recalledAbbott Medical Optics Inc. (AMO)Labeling ErrorsNationwide
DeviceCLASS IISensar 1-Piece IOL recalled by Abbott Medical Optics Inc.Abbott Medical Optics Inc. (AMO)Labeling ErrorsNationwide
DeviceCLASS IISensar Foldable IOL with OptiEdge Design recalledAbbott Medical Optics Inc. (AMO)Labeling ErrorsNationwide
DeviceCLASS IITecnis Symfony Extended Range of Vision IOL recalledAbbott Medical Optics Inc. (AMO)Labeling ErrorsNationwide
DeviceCLASS IITecnis 1-Piece Iol with the Tecnis iTec Preloaded Delivery System recalledAbbott Medical Optics Inc. (AMO)Labeling ErrorsNationwide
DeviceCLASS IITecnis OptiBlue 1-Piece Intraocular Lens (IOL) recalledAbbott Medical Optics Inc. (AMO)Labeling ErrorsNationwide
DeviceCLASS IIAbbott Healon EndoCoat Ophthalmic Viscosurgical Device recalledAbbott Medical Optics Inc (AMO)Packaging DefectsNationwide
DeviceCLASS IIAMO Sensar Intraocular Lenses (IOLs) recalledAbbott Medical Optics Inc (AMO)Labeling ErrorsNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.