Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Advanced Medical Optics, Inc.

Advanced Medical Optics, Inc. Recalls

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

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

896

Class I (Serious)

125

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 16121–16140 of 17592 recalls

Advanced Medical Optics, Inc.: AMO Tecnis Acrylic Model ZA9003 Intraocular Lenses

The lenses are incorrectly labeled as 11 diopter lenses; these lenses are actually 22.5 diopters.

FDANov 29, 2006CT, NY, TX• Advanced Medical Optics, Inc.

GE OEC Medical Systems, Inc: OEC 8800 Flexview, 892.1650 Image-intensified fluoroscopi...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. The OEC 8800 Flexview was recalled in November 2006 due to several intermittent potential safety issues including navigation tracking inaccuracy, system lok-up, incorrect image display, incorrect dose area calculated air kerma in "film mod

FDANov 20, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC Uroview 2800, Model number A349855. Designed to pr...

Recalled in November 2006 due to several intermittent potential safety issues including navigation tracking inaccuracy, system Lok-up, incorrect image display, incorrect dose area calculated air kerma in "film mode" and "digital spot mode", and the system does not reboot.

1...805 806807808 809...880

Page 807 of 880Next

FDANov 20, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC 6800 Miniview, Image-intensified fluoroscopic x-ray s...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. The OEC 6800 Miniview was recalled in November 2006 due to several intermittent potential safety issues including navigation tracking inaccuracy, system Lock-up, incorrect image display, incorrect dose area calculated air kerma in "film mo

FDANov 20, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC 8800 Flexview, 892.1650 Image-intensified fluoroscopi...

Class IHigh

FDANov 20, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC 6800 Miniview, Image-intensified fluoroscopic x-ray s...

Class IHigh

FDANov 20, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC Uroview 2800, Model number A349855. Designed to ...

Class IIModerate

FDANov 20, 2006Nationwide• GE OEC Medical Systems, Inc

VISX INCORPORATED, A SUBSIDIARY OF AMO INC: Excimer Laser System; WaveScan WaveFront System, Software...

Firm became aware of a significant overcorrection in one eye of a patient who had received a wavefront-guided LASIK treatment at a facility in Germany. The probability of a recurrence of this error was determined to be extremely remote. To ensure that this type of incident will not happen again, a software update was developed.

FDANov 17, 2006Nationwide• VISX INCORPORATED, A SUBSIDIARY OF AMO INC

Dentsply Friadent Ceramed: XiVE S plus Screw Implant D3.0/L11, Model Number 26-0122,...

Sterility of dental implants may be compromised due to cracks in packaging/caps on vials.

FDANov 17, 2006Nationwide• Dentsply Friadent Ceramed

Taylor Desk Lamp (Environmental Lighting) – Shock Hazard (2006)

Fire/Burn Risk

This recall involves "Taylor" model burnished nickel metal desk lamp. The adjustable lamp is 16 to 24.75 inches high with adjustment points at the base, mid-shaft and shade. An "O" logo is engraved on the tube cup under the rotary power switch and the name "OTT-LITE" is engraved on the front of the base. Model number 13Z63BN9 or 13T63BN9 is printed on a black label on the underside of the base.

CPSCNov 16, 2006Nationwide• Environmental Lighting Concepts Inc., of Tampa, Fla.

MRL, Inc., A Welch Allyn Company: Welch Allyn PIC 50 Portable Intensive Care System, Multi-...

Shock Delay:The monitor-defibrillator may display an 'ECG Comm' error message on the display during use, which may prevent or cause an unacceptable delay the delivery of a defibrillation shock. This delay could result in failure to resuscitate the patient.

FDANov 15, 2006Nationwide• MRL, Inc., A Welch Allyn Company

J. Jamner Surgical Instruments, Inc.: JariTrak Table Clamp, 1 inch diameter, vertical post, Cat...

The JariTrak Table Clamp may not securely fasten to the bed rail of the OR table during set up of the retractor system. In the event that the clamp is not securely fastened to the bed rail, the system may move during surgery. The firm received several complaints from hospitals.

FDANov 14, 2006Nationwide• J. Jamner Surgical Instruments, Inc.

K-GUARD Fire Extinguishers (Ansul) – Potential Failure (2006)

Fire/Burn Risk

The recall involves K-GUARD® Wet Chemical, FLAG FIRE® KITCHEN ONE® Wet Chemical, FLAG FIRE® Water and SENTRY® Water Fire Extinguishers manufactured and shipped between May 2003 and September 9, 2005. The recall program involves pick-up tube replacements in the following extinguishers: Brand Model Part Number(s) K-GUARD® Wet Chemical K01-1 430849 (UL) 430850 (ULC) K01-2 432843 (UL) 432848 (ULC) SENTRY® Water W02-1 430847 (English) 430848 (Spanish/English) FLAG FIRE® KITCHEN ONE® Wet Chemical KS-6000 552055 (UL) 552500 (ULC) FLAG FIRE® Water PWS-25G 552050 (UL) 552501 (ULC) Model numbers can be found on the fire extinguisher labels. Affected models meet the following criteria: The year 2004 or 2005 is stamped on the hanger hook attachment on the shell. For 2003 models, information on specific serial numbers included in the recall can be found at www.ansul.com for the K-GUARD Wet Chemical and SENTRY Water extinguishers, or at www.pyrochem.com for the FLAG FIRE and KITCHEN ONE Wet Chemical extinguishers. Contact the firm to determine if your extinguisher is included in this replacement program.

CPSCNov 13, 2006Nationwide• Ansul Incorporated, of Marinette, Wis.

Conmed Corporation: FRAZIER Surgical Suction Instrument, 3 Fr. with Control V...

Firm was made aware of instances where the sterile barrier of the instruments had been compromised.

FDANov 10, 2006Nationwide• Conmed Corporation

Conmed Corporation: FRAZIER Olive Tip Suction Instrument, 10 Fr. with Control...

Firm was made aware of instances where the sterile barrier of the instruments had been compromised.

FDANov 10, 2006Nationwide• Conmed Corporation

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1; 100V -120V, 15 A (cir...

Improperly adjusting the occlusion setting may result in a pump jam error and pump stoppage.

FDANov 10, 2006Nationwide• Terumo Cardiovascular Systems Corp

Conmed Corporation: POOLE Suction Instrument, REF 0035040. MANUFACTURED FOR ...

Firm was made aware of instances where the sterile barrier of the instruments had been compromised.

FDANov 10, 2006Nationwide• Conmed Corporation

Conmed Corporation: FRAZIER Atraumatic Soft Tip Surgical Suction Instrument w...

Firm was made aware of instances where the sterile barrier of the instruments had been compromised.

FDANov 10, 2006Nationwide• Conmed Corporation

Computerized Medical Systems Inc: AccuSeed DS Digital Stepper, an accessory to a prostate r...

The In/Out adjustment knob can be over-turned, ultimately causing the incorrect placement of radioactive seeds in the patient.

FDANov 9, 2006Nationwide• Computerized Medical Systems Inc

DeWalt Framing and Circular Saws – Laceration Risk (2006)

Laceration Risk

This recall involves DeWalt DW378G and DW378GT 7 ¼-inch framing saws with date codes 200301-49 through 200637-49. The model numbers for the framing saws are located on the side of the housing. The date code is located either on the name plate or under the handle near the power cord exit. Circular saws involved in this recall have model number DC300 with date codes 200601-49 through 200637-49. The model number on the circular saw is located on the name plate on the top of the motor housing. The date code on the circular saw is located on the underside of the motor housing. Framing saws marked with a "V" on the underside of the handle near the cord set and circular saws marked with a "V" on the underside of the motor housing or under the handle where the battery is inserted have already been repaired and are not involved in this recall.

CPSCNov 8, 2006Nationwide• DeWalt Industrial Tool Co., of Towson, Md.