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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

893

Class I (Serious)

124

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 15021–15040 of 17593 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

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

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.

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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

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

Beckman Coulter Inc.: AutoMate TM Sample Processing System, P/N A20745 Basic As...

The recall was initiated because Beckman Coulter has confirmed an issue with the AutoMate Sample Processing Systems. If during the recovery from Error 81201001, a stuck sample carrier with a tube is moved backwards to the loading position, sample tube/input tray information will become mismatched for samples being loaded onto the AutoMate.

FDAMay 7, 2009Nationwide• Beckman Coulter 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

Beckman Coulter Inc.: UniCel DxC 880i, 860i,680i and 660i Synchron Access Clini...

The recall was initiated after Beckman Coulter confirmed reports of inaccurate Access Intrinsic Factor Ab test results displayed on, or printed from, the UniCel Dxl portion of an integrated workstation listed above. The problem is limited to numerical Intrinsic Factor Ab results produced on integrated systems running UniCel Dxl system software version 4.0, 4.1, or 4.2. The DxC portion of your inte

FDAMay 7, 2009Nationwide• Beckman Coulter Inc.

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

Erwin and Poseidon Beanie Hats (Ambler Mountain Works) – Choking Hazard (2009)

Choking Hazard

The Erwin Beanie is primarily green and white yarn knitted to configure a frog with white eyeballs and a red smile. The Poseidon Beanie comes in several colors of yarn and has hand sewn turtles, whales and octopus attached to the beanie. The beanies have the firm's logos "Ambler" or "A" printed on a fabric tag.

CPSCMay 5, 2009Nationwide• Ambler Mountain Works, of Canmore, Alberta, Canada

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

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

Becton Dickinson & Company: BD 20 ml Syringe Luer-Lok Tip Sterile, Do not reuse; Cata...

Potential for compromised sterility: Insufficient packaging seals.

FDAApr 30, 2009Nationwide• Becton Dickinson & Company

Disetronic Medical Systems, Inc.: Roche ACCU-CHEK Spirit insulin pump. Part numbers 454049...

The "up" and "down" buttons, which are used for changing the program in the menu or to administer additional insulin through a bolus delivery, may experience intermittent failure or completely cease to operate.

FDAApr 30, 2009Nationwide• Disetronic Medical Systems, Inc.

Philips Medical Systems (Cleveland) Inc: Dental Application on the Extended Brilliance Workspace v...

Philips Healthcare has decided to recall the Dental Application on the Extended Brilliance Workspace v4.0 and v4.0.1 due to the fact that when images are saved or filmed that contain the Curved Multi-planar Reformation Section (cMPRS) views that were created with a short curve the Right/Left annotations will be reversed.

FDAApr 27, 2009AL, AZ, AR +22 more• Philips Medical Systems (Cleveland) Inc

Conformis Inc: ConforMIS iUni ( Unicondylar Knee System ) Left Medial I...

Microscopic cracks potential for pre-mature revisions in patients implanted with the system.

FDAApr 23, 2009CA, LA, MI +1 more• Conformis Inc