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Alcon Laboratories, Inc

Alcon Laboratories, Inc Recalls

All product recalls associated with Alcon Laboratories, Inc.

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Recall Summary

Total Recalls

1000

Past Year

442

Class I (Serious)

138

Most Recent

Dec 2025

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 7201–7220 of 7663 recalls

Alcon Laboratories, Inc: Alcon Custom-Pak, part #6515-51, containing BD Beaver Min...

Individually packaged surgical blades, labeled as sterile, found with incomplete seals; blades purchased for use in custom surgical packs.

FDADec 22, 2006AR, IN, MN +3 more• Alcon Laboratories, Inc

Alcon Laboratories, Inc: Alcon Custom-Pak, part #2638-17, containing BD Beaver Min...

Individually packaged surgical blades, labeled as sterile, found with incomplete seals; blades purchased for use in custom surgical packs.

FDADec 22, 2006AR, IN, MN +3 more• Alcon Laboratories, Inc

Alcon Laboratories, Inc: Alcon Custom-Pak, part #10975-02, containing BD Beaver Mi...

Individually packaged surgical blades, labeled as sterile, found with incomplete seals; blades purchased for use in custom surgical packs.

FDADec 22, 2006AR, IN, MN +3 more

1...359 360361362 363...384

Page 361 of 384Next

• Alcon Laboratories, Inc

Boston Scientific Corporation One Boston: Wallstent Endoscopic Biliary Endoprosthesis- 8mm x 40mm, ...

Guidewire restriction during use (excessive adhesive in the guidewire lumen)

FDADec 20, 2006Nationwide• Boston Scientific Corporation One Boston

Fruit Slicer (Farberware) – Laceration Hazard (2006)

Laceration Risk

The recalled product is the Farberware® Classic Series™ Fruit Slicer and Corer with model number 78350. The model number is written on the packaging. The fruit slicer/corer is an eight-section round metal blade encircled in hard black plastic with two handles. "FARBERWARE" is printed on the top of the handle.

CPSCDec 19, 2006Nationwide• Lifetime Brands Inc., of Westbury, N.Y.

Gas Boilers (Crown) – Carbon Monoxide Risk (2006)

Fire/Burn Risk

The recall involves Bermuda BSI and Cayman CWI Series gas-fired boilers designed for indoor installation. Model and serial numbers included in this recall are listed below and are located on the rating plate. The boilers have a two-tone, red and gray jacket enclosure with the controls and piping on the right side of the unit. The rating plate is a silver label located in the upper left hand corner of the right side panel. Model Numbers BSI069SN BSI069EN BSI172SL BSI172EL CWI069SN CWI069EN CWI172SL CWI172EL Serial Numbers CROWNB000304258 and CROWNB000411446

CPSCDec 19, 2006Nationwide• Crown Boiler Co., of Philadelphia, Pa.

Terang Nusa Sdn Bhd 1, Jalan 8, Pengkalan Chepa 2, Ind Zone Kota Bharu Malaysia: Sterile Neolon 2G Latex-Free Powder-Free Neoprene Surgica...

Some of the packages labeled as latex-free actually contain latex gloves.

FDADec 18, 2006Nationwide• Terang Nusa Sdn Bhd 1, Jalan 8, Pengkalan Chepa 2, Ind Zone Kota Bharu Malaysia

Alcon Laboratories, Inc: AcrySof ReSTOR Intraocular Lens

Intraocular lenses exposed to extreme temperatures while in storage.

FDADec 14, 2006Nationwide• Alcon Laboratories, Inc

Bausch & Lomb Inc: Bausch & Lomb Millennium 20 Ga. High Speed Posterior Vitr...

Laceration Risk

The cutter tip could break during a procedure

FDADec 14, 2006Nationwide• Bausch & Lomb Inc

Bausch & Lomb Inc: Bausch & Lomb Lightning High Speed Vitrectomy Cutter, Cat...

Laceration Risk

The cutter tip could break during a procedure

FDADec 14, 2006Nationwide• Bausch & Lomb Inc

Alcon Laboratories, Inc: AcrySof Intraocular Lens

Intraocular lenses exposed to extreme temperatures while in storage.

FDADec 14, 2006Nationwide• Alcon Laboratories, Inc

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: ACS DUOSTAT Rotating Hemostatic Valve, 0.096 inch, for us...

Specific lots of the .096' and .115' Rotating Hemostatic Valves (RHV) and the Duostat .096' Rotating Hemostatic Valve (RHV) potentially have an incomplete seal in the packaging pouch

FDADec 5, 2006Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: ACS Rotating Hemostatic Valve, 0.096 inch, for use with a...

Specific lots of the .096' and .115' Rotating Hemostatic Valves (RHV) and the Duostat .096' Rotating Hemostatic Valve (RHV) potentially have an incomplete seal in the packaging pouch

FDADec 5, 2006Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

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

Goulds Pump Products – Fire Suppression Fault (2006)

Fire/Burn Risk

The recalled pumps are general in purpose, but are sometimes used in fire suppression systems. The pumps were sold under the Goulds Pumps, Bell & Gossett and Red Jacket Water Products brands. The pumps can be identified by having Model NPE, NPO, MCC, MCS, SM or Series 3530 on their nameplate. Recalled pumps were manufactured between December 2005 and September 7, 2006. They have date code M05, A06, B06, C06, D06, E06, F06, G06, H06 or J06. The date code is the first three digits of the serial number on the pump nameplate.

CPSCOct 25, 2006Nationwide• ITT Water Technology Inc., of Auburn, N.Y.

Discount Diabetic Supply: One Touch Ultra Blood Glucose test strips, LifeScan, a J...

Counterfeit-blood glucose test strips (manufacturer unknown)

FDAOct 19, 2006Nationwide• Discount Diabetic Supply

Continental Medical Labs, Inc: Fibrin Analysis Catheter Testing System includes the comp...

Fibrin Analysis Catheter Testying System contains the ''Luer Lok Access Device'' that fails to lock securely to certain catheter devices because the male luer taper surface is not within the specification of the taper.

FDAOct 18, 2006IN, WI• Continental Medical Labs, Inc

Cyberonics, Inc: Handhelds-Cyberonics VNS Therapy System, Model 250-''Hand...

During programming, pulse generator may be inadvertently set to 8.0 mA output, regardless of the mA range selected by the clinician

FDAOct 17, 2006Nationwide• Cyberonics, Inc

Cyberonics, Inc: Cyberonics VNS Therapy System, Model 250-''HAND HELD'' pr...

During programming, pulse generator may be inadvertently set to 8.0 mA output, regardless of the mA range selected by the clinician

FDAOct 17, 2006Nationwide• Cyberonics, Inc

MK 20 Scuba Regulators (Scubapro) – Service Recall (2006)

The recall involves first stage regulators that are marked with the Scubapro brand and identified as the MK20.

CPSCOct 2, 2006Nationwide• Scubapro® USA, of El Cajon, Calif.