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Olympus America Inc., of Melville, N.Y.

Olympus America Inc., of Melville, N.Y. Recalls

All product recalls associated with Olympus America Inc., of Melville, N.Y..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 23641–23660 of 25000 recalls

Olympus 35mm Film Cameras – Overheating Risk (2006)

The recall includes the Infinity Twin, AF-1 Twin, Infinity Zoom 200 series, AZ 200 series, and Quantary Infinity Zoom 222 Olympus-brand 35mm film cameras. The model name is printed on the face of the camera. These cameras have a built-in flash.

CPSCMar 14, 2006Nationwide• Olympus America Inc., of Melville, N.Y.

Karl Storz Endoscopy America Inc 600 Corporate Pointe: Storz Documentation Cart with Articulating Arm, Model Num...

THE ARTICULATING ARM ON THE CART, WHICH HOLDS THE MONITOR, MAY FALL OFF FROM THE CART DURING MANIPULATION. WHEN IT FALLS, IT COULD HIT THE GROUND OR FALL ON THE PEOPLE/OBJECTS THAT ARE IN CLOSE PROXIMITY.

FDAMar 10, 2006Nationwide• Karl Storz Endoscopy America Inc 600 Corporate Pointe

Access Point Medical LLC Three City Place Drive Suite 750 St. Louis MO 63141: Access Point Medical Canes, Cane, Off-Set Crook w/Strap-B...

1...1181 118211831184 1185...1250

Page 1183 of 1250Next

The canes were made of unacceptable materials and could break

FDAMar 10, 2006Nationwide• Access Point Medical LLC Three City Place Drive Suite 750 St. Louis MO 63141

Apple Medical Corporation: Fischer Cone Biopsy Excisor - Small Model: 900-150

Change in product material may be cause for wire breaking, and tip burning and melting during procedure. Broken pieces of the device may need to be retrieved from patient.

FDAMar 10, 2006Nationwide• Apple Medical Corporation

Apple Medical Corporation: Fischer Cone Biopsy Excisor - Dual Sets Model: 900-156

Change in product material may be cause for wire breaking, and tip burning and melting during procedure. Broken pieces of the device may need to be retrieved from patient.

FDAMar 10, 2006Nationwide• Apple Medical Corporation

Apple Medical Corporation: Fischer Cone Biopsy Excisor - Large Model: 900-152

Change in product material may be cause for wire breaking, and tip burning and melting during procedure. Broken pieces of the device may need to be retrieved from patient.

FDAMar 10, 2006Nationwide• Apple Medical Corporation

Apple Medical Corporation: Fischer Cone Biopsy Excisor - Medium Model: 900-151

Change in product material may be cause for wire breaking, and tip burning and melting during procedure. Broken pieces of the device may need to be retrieved from patient.

FDAMar 10, 2006Nationwide• Apple Medical Corporation

Apple Medical Corporation: Fischer Cone Biopsy Excisor - Lg - Shallow Model: 900-155

Change in product material may be cause for wire breaking, and tip burning and melting during procedure. Broken pieces of the device may need to be retrieved from patient.

FDAMar 10, 2006Nationwide• Apple Medical Corporation

Apple Medical Corporation: Fischer Cone Biopsy Excisor Model: 900-157

Change in product material may be cause for wire breaking, and tip burning and melting during procedure. Broken pieces of the device may need to be retrieved from patient.

FDAMar 10, 2006Nationwide• Apple Medical Corporation

Forever-Glo Nite Lites (AmerTac) – Fire Hazard (2006)

The recalled "Forever-Glo Nite Lites™" look like small picture frames that plug into the wall. Only model numbers 75001 or 75002 with a manufacture date of April 2004 or later are included in this recall. Model 75001 is white or bronze-colored and has molded scroll-work around the front of the nite lite. "Model 75001" is printed on the back of the nite lite. Model 75002 is silver-colored and has a punched tin frame. "Model C8A5" is printed on the back. Both nite lite models measure about 3 inches by 3 inches and are about ¼ inch thick. "AmerTac™" and a circle with the month and year of manufacture are indicated on the back of the nite lites.

CPSCMar 8, 2006Nationwide• American Tack & Hardware Co. Inc. (AmerTac), of Saddle River, N.J.

Abbott Laboratories MPG: ARCHITECT B12 Reagent, list 06C09-22 (4 x 100 tests), 06C...

The 30-day onboard storage information is not included in the barcode labels for these two lots. As a result, the ARCHITECT system software is unable to track how long a reagent kit has been stored onboard the ARCHITECT instrument.

FDAMar 8, 2006Nationwide• Abbott Laboratories MPG

Advanced Bionics Corporation 12740 San Fernando Rd Bldgs. 1 & 3 Sylmar CA 91342: The unimplanted HiRes90K Implantable Cochlear Stimulator...

Certain HiRes 90K cochlear implants could fail as a result of elevated moisture levels. The unimplanted HiRes 90K implants listed are being removed from the market. Patients are to be followed for signs of device failure: intermittent function, complete loss of sound, sudden discomfort, pain, noise, or popping.

FDAMar 8, 2006Nationwide• Advanced Bionics Corporation 12740 San Fernando Rd Bldgs. 1 & 3 Sylmar CA 91342

Quechua Snowboard Bindings – Fall Risk (2006)

The model Rn'x7FX Quechua snowboard bindings are white or black. The word "Quechua" is located on the back of the binding. The model number is stamped on the box. Other Quechua snowboard bindings are unaffected by the recall but consumers may bring them to the store for proper identification.

CPSCMar 3, 2006Nationwide• Decathlon USA, of Wilmington, Mass.

BD Opthalmic Systems: BD Xstar Bevel Up Slit Knife 2.8mm , Sterile Catalog Num...

Product labeled as a 2.8 mm may contain a 3.2 mm Xstar slit knife

FDAFeb 28, 2006Nationwide• BD Opthalmic Systems

Integrated Orbital Implants Inc: Bio-Eye Hydroxyapatite (HA) Orbital Implant and Conformer...

The end label on the outer box was mislabeled on 9 of a 10 unit lot. The end label says ''22 mm'' and the implants are actually ''20 mm''. The main label on the cardboard box applied by the contract packager is correct in identifying the product as ''20 mm''.

FDAFeb 27, 2006Nationwide• Integrated Orbital Implants Inc

General Electric Med. Sys. Ultrasound: Voluson 730 Expert, Voluson 730 Pro, Voluson 730 ProV wit...

In the cardiac measurement section of the device the calculation of the 'PG Mean' (mean pressure gradient) leads to an erroneous result. It is recommended that customers with affected units do not use the measurement in question 'PG Mean' for any diagnostic or therapeutic decision, and 'PG Mean' values should not be included in any patient documentation.

FDAFeb 24, 2006Nationwide• General Electric Med. Sys. Ultrasound

Merit Convenience Kits (Merit Medical) - Sterility Concerns (2006)

Lack of Assurance of Sterility: Procedure kits contain a balanced salt solution that may be contaminated with endotoxins.

FDAFeb 24, 2006CT, MD, OH +1 more• Merit Medical Systems, Inc

Toshiba American Med Sys Inc: Toshiba America Medical Systems, Ultimax System MDX-8000A...

When the error condition occurs the x-ray exposures will terminate immediately. The digital system (EPS-Plus/ADR-1000A) will immediately stop acquiring images or will continue to acquire blank images. The remote console will lock-up upon release of the hand switch. The operator must reboot the system. This will result in the loss of the images acquired during the contrast portion of the study.

FDAFeb 23, 2006Nationwide• Toshiba American Med Sys Inc

Chicken Limbo Game (Milton Bradley) – Injury Risk (2006)

The recalled "Chicken Limbo" is a plastic electronic game consisting of two red vertical poles set in yellow bases and an orange horizontal bar with a plastic white chicken at the center of the bar. The game is intended for children age 4 and up.

CPSCFeb 23, 2006Nationwide• Milton Bradley, of East Longmeadow, Mass.

Hitachi Medical Systems America Inc: Hitachi CXR-4 CT Computed Tomography X-ray System (includ...

The device has a software anomaly which affects the system's ability to create Multiplanar Reconstructions (MPR). Some images from the resulting series do not display correctly, or display at all, when MPR was run on them.

FDAFeb 21, 2006Nationwide• Hitachi Medical Systems America Inc