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Advanced Medical Optics, Inc.

Advanced Medical Optics, Inc. Recalls

All product recalls associated with Advanced Medical Optics, Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 18121–18140 of 21320 recalls

Advanced Medical Optics, Inc.: Opthalmic microsurgical system-AMO WHITESTAR SIGNATURE Ph...

Laceration Risk

AMO initiated this field correction event after becoming aware of a trend in complaints associated with AMO Vitrectomy Cutter used in conjunction with the AMO WHITESTAR SIGNATURE Phacoemulsification System. The physician may be unable to make a cut during cataract surgery.

FDAApr 2, 2008Nationwide• Advanced Medical Optics, Inc.

Stryker Communications Corp: OPHIT Optical Digital Visual Interface (DVI) Extender, P...

Product at times experiences intermittent signal loss due to electromagnetic interference.

FDAApr 1, 2008Nationwide• Stryker Communications Corp

Computerized Medical Systems Inc: Focal Radiation Treatment Planning System, Focal Release...

Focal: In absolute dose mode a beam with a port may be calculated with open normalization, with the result that the displayed dose reflects open normalization while the monitor units and QA plan reflect blocked normalization. This is particularly important when these beams also include compensators. The problem is detectable by looking at the delivered dose to the weight point in the patient as

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FDAMar 31, 2008Nationwide• Computerized Medical Systems Inc

Porex Surgical, Inc.: Ocular Conformer, Sterile, Porex Surgical Inc., 15 Dart R...

The Ocular Conformers were distributed with an expired expiration date.

FDAMar 28, 2008PA• Porex Surgical, Inc.

EMD Chemicals Inc: EMD Chemicals, Harleco Brand Ethanol Standard, 1.0 mg/ml;...

Incorrect concentration: 2 ampules measuring 2.0 mg/ml were found in a lot of 20 ampules of 1.0 mg/ml Ethanol Standard.

FDAMar 27, 2008Nationwide• EMD Chemicals Inc

Medtronic Heart Valve Division: Hall Easy-Fit Prosthetic Heart Valve - Aortic A7700. Th...

Medtronic has identified an issue with 685 Hall Easy-Fit valves Models A7700 and M7700 in which the holder of the valve was incorrectly secured to the valve. This could potentially make it difficult to easily disengage the holder from the valve.

FDAMar 25, 2008AR, CA, IL +11 more• Medtronic Heart Valve Division

Rhino Side-by-Side Vehicles (Yamaha) – brake failure risk (2008)

This recall involves model year 2008 Rhino YXR450 and YXR700 Side-by-Side Vehicles as listed below: Make/Model Primary Identification Numbers 2008 Rhino 450 YXR45FX AJ32Y-001001 ~ 001598 YXR45FHX AJ30Y-000501 ~ 000897 YXR45FSPX AJ34Y-000201 ~ 000794 2008 Rhino 700FI YXR70FX AM16Y-000101 ~ 003000 YXR70FDUX AM20Y-000101 ~ 000700 YXR70FHX AM18Y-000101 ~ 000800 YXR70FSEPX/FSP2X AM23Y-000101 ~ 001000 YXR70FSPX AM21Y-000101 ~ 001200 The Primary Identification Number is stamped on the driver's side rear tire frame rail.

CPSCMar 25, 2008Nationwide• Yamaha Motor Manufacturing Corp. of America, of Newnan, Ga.

Siemens Healthcare Diagnostics Inc.: Dimension Total Prostate Specific Antigen (TPSA) Flex Rea...

False Results: The product may exhibit falsely elevated results. The affected lots demonstrate sporadic variability in recovery of calibrator and quality control; therefore this issue may not be readily detected upon calibration or during routine processing of Quality Control.

FDAMar 24, 2008Nationwide• Siemens Healthcare Diagnostics Inc.

Smiths Medical Asd Inc: Medex MX821L 72 inch (182.9cm) Administration Sets, Stand...

Misbranded/mispackaged device was distributed. Product labeled to contain 72 inch Standard Drip ( IV) Administration Sets, actually contained 60 inch (IV) administration sets with a' Y' site.

FDAMar 24, 2008IL, MN, NJ +2 more• Smiths Medical Asd Inc

Philips Medical Systems North America Co. Phillips: Philips OmniDiagnost Eleva X-Ray System is a diagnostic i...

Unexpected movement of the X-ray table may occur. These movements may lead to patient injury, e.g., an uncontrolled tilt may cause the patient to slip off.

FDAMar 22, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Siemens Medical Solutions USA, Inc.: Sonoline Antares 5.0 ultrasound system at SW revision 200...

Software issue may result in distorted images and inaccurate measurements, which could lead to a misdiagnosis.

FDAMar 21, 2008AZ, CA, FL +33 more• Siemens Medical Solutions USA, Inc.

Roche Diagnostics Corp.: Roche/Hitachi Modular Analytics System, Modular D2400 Mod...

Possible mismatch between patient and result.

FDAMar 21, 2008Nationwide• Roche Diagnostics Corp.

Siemens Medical Solutions USA, Inc.: ACUSON Antares 5.0 ultrasound system at SW revision 200.0...

Software issue may result in distorted images and inaccurate measurements, which could lead to a misdiagnosis.

FDAMar 21, 2008AZ, CA, FL +33 more• Siemens Medical Solutions USA, Inc.

Biomet Microfixation, Inc.: Lactosorb Trauma Plating System, part numbers: 915-2100, ...

The outer foil pouch on the Lactosorb Plate system was not properly sealed. The product is labeled as sterile, but the lot was not sterilized. These devices are intended to be implanted into bone and are required to be sterile. A heavy bioburden would increase the potential for bone infection (osteomyelitis).

FDAMar 19, 2008CA, GA, HI +5 more• Biomet Microfixation, Inc.

Stryker Howmedica Osteonics Corp.: X-Celerate Universal Block Pegless Size #3, Non Sterile;

Discovery of the potential for Pin and Punch interference of the Size 3 Scorpio Notch Preparation Guide that may result in damage to bone if a user aggressively attempts to seat an obstructed punch.

FDAMar 18, 2008Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Universal Notch Preparation Guide, Size #3; Non Sterile; ...

Discovery of the potential for Pin and Punch interference of the Size 3 Scorpio Notch Preparation Guide that may result in damage to bone if a user aggressively attempts to seat an obstructed punch.

FDAMar 18, 2008Nationwide• Stryker Howmedica Osteonics Corp.

Diagnostic Chemicals, Ltd.: Diagnostics Chemical Limited Iron Assay Catalog Number: ...

Precipitate in product may cause elevated background absorbance interference.

FDAMar 14, 2008Nationwide• Diagnostic Chemicals, Ltd.

Edwards Lifesciences AG Parque Industrial Itabo Km. 18.5 Carr. Sanchez Haina, San Cristobal Dominican Republic: Edwards Lifesciences "VAMP Jr" (Venous Arterial blood Man...

Edwards Lifescience initiated a recall of on Edwards "VAMP Jr" Pressure Monitoring Products manufactured between 8/01/06 and 2/29/08 due to the potential for the cap on the reservoir of the "VAMP Jr" to become disconnected.

FDAMar 14, 2008PR• Edwards Lifesciences AG Parque Industrial Itabo Km. 18.5 Carr. Sanchez Haina, San Cristobal Dominican Republic

Merit Medical Systems, Inc.: CABG PACK, Surgical Convenience Kit, Sterile, Reorder #:K...

Component of convenience kit may not be sterile.

FDAMar 14, 2008OR, PA• Merit Medical Systems, Inc.

Philips Medical Systems North America Co. Phillips: AD 7 Patient table supplied with Allura Xper FD10 and All...

Potential for radiologic patient table to become immobile and unable to move again due to force sensor sensitivity to electromagnetic radiation.

FDAMar 14, 2008Nationwide• Philips Medical Systems North America Co. Phillips