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Computerized Medical Systems Inc

Computerized Medical Systems Inc Recalls

All product recalls associated with Computerized Medical Systems Inc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

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 17321–17340 of 21320 recalls

Computerized Medical Systems Inc: XiO Radiation Treatment Planning System, XiO Release 4.3....

In XiO, when the beams are renumbered, it is possible to get into a state where the dose displayed for a beam does not match the beam placement on the patient. This can occur when dose is calculated, beams are renumbered, and the dose is re-summed only.

FDAMay 13, 2009Nationwide• Computerized Medical Systems Inc

Boston Scientific Corporation: Boston Scientific Fort Guide Wire, Floppy Marker Wire, 30...

Product packaged incorrectly. One batch/lot of wires, that should contain radiopaque marker bands, is missing the marker bands; and a second batch/lot of wires, which should not contain radiopaque marker bands, has the marker bands. Since the marker bands issue would not be visually apparent to the physician there is a potential for prolongation or delay of the procedure in order to exchange the

FDAMay 12, 2009AR, CA, FL +2 more• Boston Scientific Corporation

Philips Medical Systems North America Co. Phillips: Accessory Cart for The ACHIEVA 3.0T and Panorama 1T Magne...

1...865 866867868 869...1066

Page 867 of 1066Next

The Accessory Cart contained magnetic material and is attracted to the magnet when bringing it close to the system.

FDAMay 12, 2009Nationwide• Philips Medical Systems North America Co. Phillips

Toshiba American Medical Systems Inc: PET-511BTM Multi-plane transesophageal transducer (TEE) u...

Toshiba America Medical Systems Inc is removing the PET-511BTM Multi-plane Transesophageal Transducer from the market after receiving several reports of injury regarding the transducer. Bending or buckling of the flexible portion of the PET-511 BTM multi-plane transesophageal transducer (TEE) may result in injury including perforation.

FDAMay 11, 2009Nationwide• Toshiba American Medical Systems Inc

Acist Medical Systems: ACIST Automated Manifold Kit , REF Model BT2000, SKU # 01...

ACIST Medical Systems initiated a recall due to an increase in the incidence of field reports related to a bulge on the side and/or leaks in the bond of the 2.5 high-pressure tubing of BT2000 kits during a procedure which can result in unsatisfactory performance of the ACIST BT2000 Automated Manifold Kit.

FDAMay 11, 2009AL, AZ, AR +39 more• Acist Medical Systems

Varian Medical Systems Oncology Systems: Varis, Aria Radiation Oncology - Version 8.1.15, 8.5.11, ...

Potential mistreatment-- due to software issues, retired plans may be used and treated repeatedly.

FDAMay 8, 2009Nationwide• Varian Medical Systems Oncology Systems

Essential Medical Supply, Inc.: Essential Medical Supply brand Essential Rollator with Lo...

The caster may separate from the frame completely causing injury to the user.

FDAMay 8, 2009Nationwide• Essential Medical Supply, Inc.

Stryker Communications Corp: Surgical Table Headrest, Catalog/Part #0788-300-012, comp...

Potential for health care provider/hospital staff member to sustain injury to fingers or hands when removing/handling the headrest component of the VERTIER Surgical Table.

FDAMay 8, 2009Nationwide• Stryker Communications Corp

GE Medical Systems, LLC: Datex-Ohmeda S/5 Device Interfacing Solution, N-DISVENT 0...

GE Healthcare has recently become aware of an issue in the calculations associated with Datex-Ohmeda S/5 Device Interfacing Solution N-DISVENT-02 interfaced between certain Datex-Ohmeda patient monitors (Datex-Ohmeda S/5 Anesthesia Monitor (AM), Datex-Ohmeda S/5 Critical Care Monitor (CCM), Datex-Ohmeda S/5 Compact Anesthesia Monitor (CAM), Datex-Ohmeda S/5 Compact Critical Care Monitor (CCCM)) an

FDAMay 8, 2009AL, AK, AZ +34 more• GE Medical Systems, LLC

Boston Scientific Corporation: Neuroform 3 Microdelivery Stent System, Model Number M003...

Mislabeling-- Product was placed in a carton, which has printed on it the name of another product. A correct product label was placed on the carton.

FDAMay 8, 2009Nationwide• Boston Scientific Corporation

Depuy Orthopaedics, Inc.: DePuy P.F.C. Sigma Knee System, Non-Porous Cruciate Retai...

There may be a crack on the lateral side of the condyle in the posterior chamfer region. The device is used as a Orthopedic knee implant.

FDAMay 7, 2009Nationwide• Depuy Orthopaedics, Inc.

Off-Road Motorcycles (KTM) – Front Fork Failure (2009)

This recall involves model year 2009 KTM off-road motorcycles. The model name and KTM™ logo are located on the right and left shrouds. The following models are included in this recall:Model Name Description 125SX Orange / Black 150SX Orange / Black 250XC-W Orange / Black 300XC-W Orange / Black

CPSCMay 7, 2009Nationwide• KTM North America Inc., of Amherst, Ohio

Torcofix/Torcoflex Torque Wrenches (Richard Abraham Herder) – Injury Risk (2009)

The wrenches were sold under three styles names: Richard Abraham Herder KG "Gedore/Rahsol" label, the Mountz "Titan" label, and the Mountz "Erico" label. Only wrenches with the serial numbers within the following ranges are included in the recall: From serial no. To serial no. 1268368 1341104 A003977 A039760 B000493 B032301 C000001 C017795 E000001 E020205 F000001 F013249 H000001 H000128 2174340 2230753 Recalled wrenches include the following product/brand names and model numbers: Product/Brand Name Model Nos. GEDORE/RAHSOL TORCOFIX K with Ratchet 4550-10; 4550-20; 4550-30; 4550-40 GEDORE/RAHSOL TORCOFLEX K with Ratchet 3550-07; 3550-10; 3550-20; 3550-30; 3550-2006 GEDORE/RAHSOL TORCOFIX Z with Spigot 4410-01; 4420-01; 4430-01; 4440-01 GEDORE/RAHSOL TORCOFIX SE with rectangle holder 4100-01; 4200-02; 4201-01; 4300-01; 4301-01 GEDORE/RAHSOL TORCOFIX K US with Ratchet 6550-15; 6551-07; 6551-10; 6551-30; 6551-60 MOUNTZ TITAN with Ratchet 280012; 280013; 280014 MOUNTZ TITAN with Spigot 280022; 280023; 280024 MOUNTZ ERICO ELT110D with Ratchet ELT110D The serial number is printed on the side of every torque wrench and the model number is printed on the label on the front and the back of the steel tube.

CPSCMay 6, 2009Nationwide• Richard Abraham Herder KG, of Solingen, Germany

Boston Scientific Corp: Boston Scientific EndoVive 24F (8 mm) Safety PEG Kit, Pus...

The user may be unable to pass the device over the guidewire for placement in the patient, resulting in an inability to use the device.

FDAMay 5, 2009Nationwide• Boston Scientific Corp

Boston Scientific Corp: Boston Scientific EndoVive 20F (6.7 mm) Safety PEG Kit, P...

The user may be unable to pass the device over the guidewire for placement in the patient, resulting in an inability to use the device.

FDAMay 5, 2009Nationwide• Boston Scientific Corp

GE Medical Systems, LLC: GE Healthcare, CT Perfusion 4 on Advantage Workstation, C...

GE Healthcare has recently become aware of the need to adjust default settings associated with the use of CT Perfusion 4 on the Advantage Workstation, ST and PET/CT consoles that may impact patient safety. The default parameter settings in CT Perfusion 4 may not be optimal in the case of data acquired with longer time sampling intervals such as axial scans with inter scan delay (ISD) greater th

FDAMay 4, 2009AZ, CA, CT +17 more• GE Medical Systems, LLC

Siemens Medical Solutions USA, Inc: Mavig Portegra 2 which is an accessory to the Siemens ang...

Improper installation of accessory support arm, which could potentially result in the loosening of the arm over time causing it to fall.

FDAMay 1, 2009Nationwide• Siemens Medical Solutions USA, Inc

GE Medical Systems, LLC: HiSpeed X/i Computed Tomography operator consoles with th...

It was discovered that the operator console did not have a label affixed in accordance with 21CFR 1010.2 indicating certification to applicable performance standards.

FDAMay 1, 2009AL, CA, CT +9 more• GE Medical Systems, LLC

Kamiya Biomedical Company, LLC: "K-ASSAY CRP (3) Calibrator E". This product is an IVD ...

The long-term stability of level 2 (1.0 mg/dL) may not be within the specifications due to a decrease in CRP concentration.

FDAMay 1, 2009Nationwide• Kamiya Biomedical Company, LLC

Philips Medical Systems North America Co. Phillips: The product's marketing brochure states: "1.5T coils and ...

Fire/Burn Risk

Combined use of the Synergy Flex-M / Shoulder Coil 1.5T increases the chance of RF interaction and heating up of the coil. This may result in possible burns of the patient.

FDAMay 1, 2009Nationwide• Philips Medical Systems North America Co. Phillips