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Toshiba American Medical Systems Inc

Toshiba American Medical Systems Inc Recalls

All product recalls associated with Toshiba American Medical Systems Inc.

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Recall Summary

Total Recalls

1000

Past Year

583

Class I (Serious)

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 9481–9500 of 10937 recalls

Toshiba American Medical Systems Inc: Toshiba CT systems, Asteion and Aquilion, that are equipp...

The systems all have a similar table control board. It has been found that this board may cause the table position to be incorrect if the table cradle is moved manually. This is referred to as "Free" mode in the operation manuals. If this error does occur it is possible that the patient could be scanned at an incorrect position.

Class IIModerate

FDAFeb 27, 2008Nationwide• Toshiba American Medical Systems Inc

Smiths Medical MD, Inc.: Deltec Micro 3100 Large Volume Infusion Pump, CE 0473, RX...

The Deltec, Graseby, and 3M, Large Volume Infusion Pump - Models 3000 and 3100, may deliver an unintended bolus if the pump door is opened and then immediately closed. This problem is due to a timing delay when the pumping mechanism resets itself.

FDAFeb 27, 2008AL, AZ, AR +43 more• Smiths Medical MD, Inc.

Hitachi Medical Systems America Inc: EUB-5500 VISION 5500 Diagnostic Ultrasound Scanner w/Step...

1...473 474475476 477...547

Page 475 of 547Next

Miscalculation reading. A software error in the firm's EUB-5500/HI VISION diagnostic scanning system causes a miscalculation of the left ICA/CCA ratio when using the Carotid Calculation package for patient scans.

FDAFeb 25, 2008Nationwide• Hitachi Medical Systems America Inc

Edwards Lifesciences Research Medical, Inc.: Edwards Lifesciences LLC, Fem-Flex II Femoral Venous Cann...

Femoral Venous Cannula was color coded as an arterial cannula. This problem could result in a minor delay in the procedure. In the worst case, this product could be connected incorrectly during bypass, which would result in a more significant delay and has the potential to result in a permanent injury.

FDAFeb 25, 2008Nationwide• Edwards Lifesciences Research Medical, Inc.

Civco Medical Instruments Inc: MT-APSD-2.4 Type-S Thermoplastic Mask, Medical charged-pa...

Mislabeled: The mask is mislabeled with the incorrect part number but the outer packaging is correct.

FDAFeb 25, 2008CA, CO, IL +7 more• Civco Medical Instruments Inc

GE OEC Medical Systems, Inc: OEC 9800; OEC FluoroTrak 9800 Plus; OEC 9800 Plus; OEC 98...

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 vertical lift column power supply in the mainframe C-arm of the device is defective and subject to early life failure.

Class IHigh

FDAFeb 22, 2008Nationwide• GE OEC Medical Systems, Inc

Smiths Medical MD, Inc.: CADD-MS"3 Ambulatory Infusion Pumps, Model 7400, Rx only...

Smiths Medical has received reports that the device powers down without an alarm. Investigation concluded that if the battery cap is not fully tightened, the pump may power down and a brief "chirp" will sound. This may occur if the user has not sufficiently tightened the battery cap or if the battery cap is damaged. If a patient is asleep or does not regularly check their Pump, there is a potentia

FDAFeb 22, 2008AZ, CA, FL +16 more• Smiths Medical MD, Inc.

GE OEC Medical Systems, Inc: OEC 9800; OEC FluoroTrak 9800 Plus; OEC 9800 Plus; OEC 98...

FDAFeb 22, 2008Nationwide• GE OEC Medical Systems, Inc

Smiths Medical MD, Inc.: Deltec Cozmo Insulin Pump, model 21-1700. A syringe infus...

Smith Medical has received reports of Deltec Cozmo Insulin Pumps powering down without an alarm. Investigation concluded that if the battery cap is not fully tightened, the Pump may power down and a brief "chirp" will sound. This may occur if the user has not sufficiently tightened the battery cap or if the battery cap is damaged. If a patient is asleep or does not regularly check their blood g

FDAFeb 22, 2008AL, AK, AZ +49 more• Smiths Medical MD, Inc.

Terumo Cardiovascular Systems Corporation: Terumo Sarns Sternal Saw II System Power Unit, 115 V, Ter...

The drive power cable cannot be fully inserted into the power unit or can only be inserted with difficulty, resulting in the device not being operational.

FDAFeb 14, 2008Nationwide• Terumo Cardiovascular Systems Corporation

Polaris ATVs - Fire Hazard (2008)

Fire/Burn Risk

This recall involves select 2005 through 2006 model Polaris Sportsman and Scrambler 500 ATVs. The model and serial numbers are printed on a decal attached to the front side of the radiator (Sportsman) or the top of the front cab cover (Scrambler 500). Serial numbers are permanently stamped into the left frame rail behind the left front wheel. The recalled models are listed on the chart below. Model Year Market Name Model Number 2004 SPRTSMN 500 A04CH50AO 2004 SPRTSMN 500 A04CH50AR 2004 SPRTSMN 500 A04CH50AS 2005 INT 500 HO A05MH50FB 2005 SCRMBLR 500 4X4 A05BG50AA 2005 SPRTSMN 400 A05MH42AB 2005 SPRTSMN 400 A05MH42AG 2005 SPRTSMN 400 A05MH42AH 2005 SPRTSMN 500 A05MH50AB 2005 SPRTSMN 500 A05MH50AC 2005 SPRTSMN 500 A05MH50AG 2005 SPRTSMN 500 A05MH50AH 2005 SPRTSMN 500 A05MH50AL 2005 SPRTSMN 500 A05MH50AT 2005 SPRTSMN 600 A05MH59AK 2005 SPRTSMN 600 A05MH59AN 2005 SPRTSMN 6X6 A05CL50AA 2005 SPRTSMN 6X6 MIL A05CL50MA 2005 SPRTSMN 700 A05MH68AD 2005 SPRTSMN 700 A05MH68AK Model Year Market Name Model Number 2005 SPRTSMN 700 A05MH68AN 2005 SPRTSMN 700 MIL A05MH68MB 2005 SPRTSMN MV7 A05MH68AP 2005 SPRTSMN MV7 A05MH68CA 2005 SPRTSMN MV7 A05MH68MA 2006 INT SPTSMAN 500 A06MH50FB 2006 SCRMBLR 500 4X4 A06BG50AA 2006 SPRTSMN 450 A06MH46AA 2006 SPRTSMN 450 A06MH46AC 2006 SPRTSMN 450 A06MH46AD 2006 SPRTSMN 450 A06MH46AF 2006 SPRTSMN 450 A06MH46AT 2006 SPRTSMN 500 A06MH50AA 2006 SPRTSMN 500 A06MH50AB 2006 SPRTSMN 500 A06MH50AD 2006 SPRTSMN 500 A06MH50AF 2006 SPRTSMN 6X6 A06CL50AA 2006 SPRTSMN 700 A06MH68AA 2006 SPRTSMN 700 A06MH68AD 2006 SPRTSMN 700 A06MH68AF

CPSCFeb 14, 2008Nationwide• Polaris Industries Inc., of Medina, Minn.

GE Medical Systems, LLC: Revolution XR/d system control room PC model 5117866-2 wi...

GE Healthcare has recently become aware of a potential risk of observing a blank image after exposure on Revolution XR/d systems equipped with HP 8200 PC user consoles that may impact patient safety. It was reported that images acquired with off-center collimation for extremities with the position selected as Digits to front or Digits to back are displayed as blank. Investigation into th

FDAFeb 14, 2008Nationwide• GE Medical Systems, LLC

Impac Medical Systems Inc: SEQUENCER, MOSAIQ versions 1.3 and 1.4 with Elekta and Si...

Software issue may result in change to intended treatment field, potentially resulting in mistreatment.

FDAFeb 14, 2008AL, AZ, CA +18 more• Impac Medical Systems Inc

GE Medical Systems, LLC: Revolution XR/d systems with control room PC model 511786...

GE Healthcare has recently become aware of an error in the generator software on the Revolution XR/d configured with HP 8200 PC consoles that reports a mAs reading that is higher than is actually exposed to patients.

FDAFeb 14, 2008AL, AZ, CA +20 more• GE Medical Systems, LLC

Varian Medical Systems Oncology Systems: Eclipse Treatment Planning System, Client 8.1.18 and DCF ...

A software error causes the wedge accessory calculation to be ignored in the radiotherapy treatment plan.

FDAFeb 13, 2008AL, AZ, AR +24 more• Varian Medical Systems Oncology Systems

Hitachi Medical Systems America Inc: Altaire MRI System Emergency Rundown Switch Unit (ERDU) i...

The firm's Altaire MR Scanner's Emergency Rundown Switch Unit (ERDU), that is used to shut down the device in an emergency, was found to be defective. An ERDU failure could delay or prevent patient access leading to possible patient death or serious injury.

FDAFeb 11, 2008Nationwide• Hitachi Medical Systems America Inc

Transparent Egg Shakers (West Music) - Choking Risk (2008)

Choking Hazard

This recall involves clear, plastic egg-shaped instruments with various color beads inside. The beads inside the shaker instrument come in five colors: red, white, green, dark blue and aqua. "Basic Beat" and "Jumbo Egg Crystal" is printed on a label attached to the plastic bag packaging. Model numbers "BB5102" and "202212" are printed on the side of the label.

CPSCFeb 7, 2008Nationwide• West Music Company, of Coralville, Iowa

Philips Medical Systems North America Co. Phillips: Philips Gallileo Automatic Collimator, Part Numbers: 9896...

The collimator could fall from the x-ray stand, due to loosening screws, and strike a patient or operator underneath.

FDAFeb 7, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Terumo Cardiovascular Systems Corporation: Terumo Sarns cardiovascular disposable products, Weighted...

A loose strand of stainless steel left on the device during manufacturing may result in an unretrieved metal fragment remaining in the patient.

FDAFeb 5, 2008Nationwide• Terumo Cardiovascular Systems Corporation

Medtronic Neuromodulation: IsoMed Refill Kit, Model 8553, Lot Number 60538731, is in...

Medtronic is retrieving all unused packages of ISOMED Refill Kit Model 8553, Lot 60538731. This lot of product was released using incorrect endotoxin specification limits. Endotoxin contamination can potentially lead to fever, malaise, respiratory distress, septic shock, and death.

FDAFeb 4, 2008AL, AK, AZ +34 more• Medtronic Neuromodulation