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Otsuka America Pharmaceutical, Inc.

Otsuka America Pharmaceutical, Inc. Recalls

All product recalls associated with Otsuka America Pharmaceutical, Inc..

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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 22881–22900 of 25000 recalls

Otsuka America Pharmaceutical, Inc.: UBiT-IR300 Infrared Spectrophotometer, Software Versions ...

Medical device power supply may overheat and cause smoke to be emitted from the device.

FDAJan 18, 2008Nationwide• Otsuka America Pharmaceutical, Inc.

Radiometer America Inc: ABL800 FLEX Series Analyzer - Human Blood Analyzer (Labor...

Reported calibration errors are not displayed on the analyzers parameter bar screen or on the patient results when the calibration number is between 32768 - 65535 and 98303 - 131070. This may cause the operator to perform measurements and obtain questionable results.

FDAJan 18, 2008IN• Radiometer America Inc

Civco Medical Instruments Inc: CIVCO Latex-Free Needle Guide, Sterile transrectal needle...

Incorrect Needle Guide- The individual pouches contained V53W Endocavity Needle guide(p/n/034-054) instead of the Shimadzu T/R Needle guide (p/n134-054).

1...1143 114411451146 1147...1250

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FDA

Jan 16, 2008

Nationwide

• Civco Medical Instruments Inc

St Jude Medical CRMD: Implantable Cardioverter Defibrillator EPIC VR Tiered-th...

A condition that could lead to a ventricular sensing anomaly in Epic and Atlas family of lmplantable Cardioverter Defibrillators (ICDs) has been identified. A loss of ventricular sensing would prevent the ICD from being able to detect an arrhythmia. If an arrhythmia occurred and the device was unable to detect it, then a patient would not receive potentially life saving therapy.

FDAJan 16, 2008Nationwide• St Jude Medical CRMD

John Deere Compact Utility Tractors – collision hazard (2008)

The recalled tractor is model number 3203, which is painted on the side of the tractor. The recall includes the following serial numbers: LV3203H000001 through LV3203H000010 LV3203H190001 through LV3203H193434 LV3203H393093 LV3203H394001 through LV3203H396669 The serial number plate is located on the tractor's frame above the right front wheel.

CPSCJan 16, 2008Nationwide• Deere & Company, of Moline, Ill.

Toy Wrestler Figures (A.A. of America) – lead paint violation (2008)

The recalled toy is a package of four action figures. Each figure is about 5 3/4 inches high. The UPC number 604111230003 is printed on the product's packaging.

CPSCJan 15, 2008Nationwide• A.A. of America Inc., of East Brunswick, N.J.

Terumo Cardiovascular Systems Corporation: Terumo Sarns Level Sensor II Pads. For use with Sarns Ad...

The level sensor holder may detach from the adhesive pad causing the sensor to lose contact with the venous reservoir, which may result in a detached sensor indication or false alarm.

FDAJan 13, 2008Nationwide• Terumo Cardiovascular Systems Corporation

Straumann Usa, Llc: Straumann NC Closure Screw, Titanium, Precision attachmen...

Mislabeled package: Narrow Connection (NC) Closure Screws contain closure screws for the regular connection (RC) bone level implant. The RC closures screw is larger (3.5mm diameter) and therefore, will not fit into the NC implant (3.0mm diameter) narrow connection.

FDAJan 10, 2008Nationwide• Straumann Usa, Llc

Whole-house Exhaust Fan Motors (A.O. Smith) – Fire Hazard (2008)

Fire/Burn Risk

The recalled electric motor is part of a residential whole-house exhaust fan that is typically mounted on the floor of an attic. The shutters of the fan are visible on the ceiling of the floor beneath the attic and must be opened and closed by the consumer. The motors were included with exhaust fans manufactured and distributed by Air Vent Inc. and Triangle Engineering of Arkansas Inc. "A.O. Smith," the model number, and the service date code are printed on the rating plate of the motor. The recall includes model numbers S56A30A54 and S56A30A97, and service date codes 032076M - 334076M, 03207JY - 33407JY, and YB07 - YL07. Units that have a sticker indicating that the unit has been rewired are not subject to this recall.

CPSCJan 10, 2008Nationwide• A.O. Smith Electrical Products Co., of Tipp City, Ohio

Intermatic DT27 Digital Timers – Electrical Shock Risk (2008)

This recall involves the Intermatic DT27 digital self-adjusting timer with a date code of "04B." This product is a lamp and appliance timer and is packaged as either the "DT27C Heavy Duty Digital Timer" or the "DT27CL Time All® Digital Lamp and Appliance Self-Adjusting Timer." The timer is white with a rounded top, and measures 3 7/8" tall by 2 3/4" wide by 1 5/8" deep. The brand name "Intermatic" is molded on the front of the timer, and the model number ("DT27") and date code ("04B") are printed on the back of the timer.

CPSCJan 9, 2008Nationwide• Ewig Industries Macao Commercial Offshore Ltd., of Macau, China

Honda TRX 500 ATVs – Speed Control Failure (2008)

This recall involves Model Year 2007 Honda TRX 500 ATVs, also known as the Honda Foreman and Foreman Rubicon. The adult-size ATVs are designed for use by riders age 16 and older. The 2007 model year ATVs are available in red, black, blue, olive, and camouflage. The Honda name and wing logo are printed on the fuel tank and the model name is printed on the side panel just below the seat.

CPSCJan 9, 2008Nationwide• American Honda Motor Co., Inc. of Torrance, Calif.

Trailer Bicycles (Pacific Cycle) – Detachment Risk (2008)

The "Pathfinder," "Run About," and "Alley Cat" are single-wheeled, children's bicycles that connect to an adult's bicycle by a coupler. The recall includes model numbers: 12-PF250, 13-SC250, 13-SC350 and M5101. The model number is located on the lower seat tube of the frame. The affected couplers have welded plates; bicycles that have couplers with cast parts are not included in this recall.

CPSCJan 8, 2008Nationwide• Pacific Cycle Inc., of Madison, Wis.

Highland Metals: Stainless Steel, Natural, Upper, .018": Arch Wires. Highl...

Boxes of stainless steel orthodontic wires were mislabeled with the incorrect size.

FDAJan 7, 2008Nationwide• Highland Metals

Highland Metals: Stainless Steel, Progressive Lower, .016: Arch Wires. In...

Boxes of stainless steel orthodontic wires were mislabeled as size.018"

FDAJan 7, 2008Nationwide• Highland Metals

Highland Metals: Stainless Steel, Natural,Lower, .016 x.022: Arch Wires. H...

Boxes of stainless steel orthodontic wires were mislabeled with the incorrect size.

FDAJan 7, 2008Nationwide• Highland Metals

Philips Medical Systems North America Co. Phillips: EasyDiagnost Classic has a radiographic tilting table. T...

Potential for the tower (holding the serial changer and/or image intensifier) to slide unexpectedly and potentially injure a patient or user in its path.

FDAJan 4, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Easy Diagnost DSI is a Easy Diagnost Digital Spot Imaging...

Potential for the tower (holding the serial changer and/or image intensifier) to slide unexpectedly and potentially injure a patient or user in its path.

FDAJan 4, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Philips Healthcare Informatics, Inc.: iSite PACS image management system; Picture Archiving and...

Incorrect display of one of the patient's images. This malfunction could cause an image to be incorrectly displayed, for example flipped left to right and anterior to posterior. The original image is still presented in the correct orientation next to the incorrect image when displayed on the monitor.

FDAJan 4, 2008Nationwide• Philips Healthcare Informatics, Inc.

Philips Medical Systems North America Co. Phillips: Diagnost 56/66/76/76 Plus, DSI is a Spot-Film and has a D...

Potential for the tower (holding the serial changer and/or image intensifier) to slide unexpectedly and potentially injure a patient or user in its path.

FDAJan 4, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Varian Medical Systems Oncology Systems: Varian Medical Systems On-Board Imager, Versions 1.0.15 a...

If used with a third party radiation therapy treatment planning software system, mistreatment may occur because of a misalignment.

FDAJan 3, 2008AL, AK, AZ +35 more• Varian Medical Systems Oncology Systems