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Kamiya Biomedical Company

Kamiya Biomedical Company Recalls

All product recalls associated with Kamiya Biomedical Company.

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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 24361–24380 of 25000 recalls

Kamiya Biomedical Company: K-Assay Lp(a) Control

Assay result not consistent with the assigned control value

FDAMar 29, 2004CA, GA, IN +3 more• Kamiya Biomedical Company

General Electric Med Systems: Advantx 1 LC1 Model 46-279781P1 Angiographic X-ray System

Unintended movements of both the C-arc and the image intensifier have occured due to shearing of the gear motor shaft as a result of the misalignment of the gearbox.

FDAMar 24, 2004Nationwide• General Electric Med Systems

General Electric Med Systems: Advantx 1 LC1 Model 45258230 Angiographic X-ray System

Unintended movements of both the C-arc and the image intensifier have occured due to shearing of the gear motor shaft as a result of the misalignment of the gearbox.

FDAMar 24, 2004Nationwide

1...1217 121812191220 1221...1250

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• General Electric Med Systems

General Electric Med Systems: Advantx 1 LC2 Model 2105657 Angiographic X-ray System

Unintended movements of both the C-arc and the image intensifier have occured due to shearing of the gear motor shaft as a result of the misalignment of the gearbox.

FDAMar 24, 2004Nationwide• General Electric Med Systems

General Electric Med Systems: Advantx 1 LC2 Model 45562281 Angiographic X-ray System

Unintended movements of both the C-arc and the image intensifier have occured due to shearing of the gear motor shaft as a result of the misalignment of the gearbox.

FDAMar 24, 2004Nationwide• General Electric Med Systems

General Electric Med Systems: Advantx 1 SC Model 36006617 Angiographic X-ray System

Unintended movements of both the C-arc and the image intensifier have occured due to shearing of the gear motor shaft as a result of the misalignment of the gearbox.

FDAMar 24, 2004Nationwide• General Electric Med Systems

Isabella Cribs (Stanley Furniture) – Structural Problem (2004)

These are Isabella model cribs with model number 326-94C1 or 326-94C2. The model number appears on the bar code label. The Isabella cribs are distributed through Stanley Funiture's Young America line. They are made of wood and painted white.

CPSCMar 24, 2004Nationwide• Stanley Furniture Company Inc., Stanleytown, Va.

Philips Medical Systems (Cleveland) Inc: AcQSim X-Ray Computed Tomography Scanners. These scanners...

Software anomaly in the DICOM Modality Worklist. When restoring a patient's images from the optical disk, images from the wrong patient may be displayed.

FDAMar 23, 2004Nationwide• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc: Ultra Z 90 X-Ray Computed Tomography Scanners. These sca...

Software anomaly in the DICOM Modality Worklist. When restoring a patient's images from the optical disk, images from the wrong patient may be displayed.

FDAMar 23, 2004Nationwide• Philips Medical Systems (Cleveland) Inc

Braun, B Medical Inc: Introcan Safety IV Catheter 22G x 1'' PUR with Wings. T...

Mislabeled product. The recalling firm received a complaint that a box of Introcan Safety Catheters, (22G x 1 inch) contained mixed 18G catheters with the same lot number.

FDAMar 19, 2004Nationwide• Braun, B Medical Inc

USA Instruments Inc.: Prima III TotalSENSE Torso Coil (Body Array Coil), labele...

A defective capacitor in the Body Array Coil may result in unstable, unreliable performance, with excessive heating of patient's body.

FDAMar 19, 2004CA, CT, FL +10 more• USA Instruments Inc.

Votive Candles (Bath & Body Works) – Product Safety (2004)

The votive candles were sold individually and in sets. A label on the bottom of the votive candle reads: Real Essence 1½" x 2½". The specific recalled votive candles are: Rosewood Tea; Lilac Blossom; Vintage Leather; Brushed Suede; Warm Vanilla Sugar; Sweet Cinnamon Pumpkin; Spiced Cider; and Amber Myrrh. These votive candles were also sold in a six-pack set: Lilac Blossom, Spiced Cider, and Sweet Cinnamon Pumpkin. In addition, Sweet Cinnamon Pumpkin was sold in "the scented home quartet" set. This recall does not apply to any other Real Essence votive candles.

CPSCMar 18, 2004Nationwide• Bath and Body Works, of Columbus, Ohio

Toshiba American Med Sys Inc: Computed Tomography, Models TSX-101A and TSX-021A.

Erroneous patient data is entered. Previoius patient's demographics are recorded.

FDAMar 17, 2004Nationwide• Toshiba American Med Sys Inc

Sun-Sational Electric Heater (Lakewood) – Safety Issue (2004)

The recalled "Sun-Sational" Deluxe Radiant heaters have a metallic gray heating element, white base, and red control knobs. The heater has a label at the base, that reads "SUN-sational" and "Warning: Risk of Fire." The oval-shaped heater has an 800-Watt and 1200-Watt setting and has a sensor to alert users of overheating.

CPSCMar 17, 2004Nationwide• Lakewood Engineering and Manufacturing Co., of Chicago, Ill.

Poof Chairs (Palliser Furniture) – Design Risk (2004)

Laceration Risk

This set includes two semi-circular chairs and one circular table in blue, red, and yellow fabric. The law label on the bottom of the chair has "Hong Feng Furniture Cushion Co." and "Palliser Furniture Ltd."

CPSCMar 17, 2004Nationwide• Palliser Furniture Ltd., Winnipeg, Manitoba, Canada

Alabaster Wall Sconces (Brass Light Gallery) – Installation Problem (2004)

The wall-mounted light fixtures have a translucent, natural alabaster stone cover. The recalled wall sconces include model numbers AL-3208, AL-5008, and AL-5108. Models AL-3208 and AL-5008 use one light bulb; whereas, Model AL-5108 uses two bulbs. The alabaster covers measure 8 inches in width and between 9½ and 15 inches in height.

CPSCMar 17, 2004Nationwide• Brass Light Gallery Inc., of Milwaukee, Wis.

Bayer Healthcare LLC 1884 Miles Ave Buildings 110 (Adlake), 17 & 18 Elkhart IN 46514-2291: Clinitek 50 Urine Chemistry Analyzer; Product codes 6509C...

Some units may only have had 1 read head screw installed instead of the three required by the firm's specifications.

FDAMar 12, 2004Nationwide• Bayer Healthcare LLC 1884 Miles Ave Buildings 110 (Adlake), 17 & 18 Elkhart IN 46514-2291

Portable Cord Reel (Harbor Freight) – Electrical Safety (2004)

The recalled heavy duty portable industrial cord reels are yellow with a carrying handle, extendable/retractable extension cord and 6 electrical outlets/plugs. The units are marked "Cord Reel Portable Power" and sold as "SKU 42053." The label on the rear of the unit contains the following information: "Cord Reel, 10 Amps, 125 Volts, 1250 Watts, Caution, Disconnect all plugs inserted into the outlets on this face before winding cord reel in either direction, Made in Taiwan, R.O.C."

CPSCMar 10, 2004Nationwide• Harbor Freight Tools, of Camarillo, Calif.

Hair Dryers (Light Distribution) – Electrical Safety (2004)

Laceration Risk

The recalled units are the Turbo 1650 and Turbo 2650 electric hand-held hair dryers. These hair dryers have a pistol grip, black or red and black colored plastic casing, two-prong power cord, and a label that reads in part: "Light Distribution" or "Windsor" and "110V/60HZ". The model name and number also are printed on the label.

CPSCMar 9, 2004Nationwide• Light Distribution Inc., of Miami, Fla.

Hair Dryers (Lado Co.) – Electrical Safety (2004)

Laceration Risk

The recalled units are the Formula 3000, Energy Turbo, and Rapid 1085 electric hand-held hair dryers. These hair dryers have a pistol grip, black or dark blue colored plastic casing, two-prong power cord, and a label that reads in part: "Lado Professional" and "110V/60HZ". The model name and number also are printed on the label.

CPSCMar 9, 2004Nationwide• Lado Co. of America, of Flushing, N.Y.