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Dixtal Medical, Inc.

Dixtal Medical, Inc. Recalls

All product recalls associated with Dixtal Medical, Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 31881–31900 of 37665 recalls

Dixtal Medical, Inc.: Dixtal Novametrix Neonatal/Pediatric SpO2 Sensor, Foam Wr...

Neonatal/Pediatric SPU Sensors may be incorrectly packaged in pouches labeled for Adult/Pediatric SPU Sensors.

FDAMay 13, 2009CT, TX• Dixtal Medical, Inc.

Widetrak Snowmobiles (Polaris) – Shock Hazard (2009)

This recall involves model year 2009 Polaris IQ WIDETRAK snowmobiles with the engine block or battery heater directly installed. Model number S09PU7ES is printed on the right side of the tunnel below the seat. This recall also involves Polaris accessory engine block heaters and battery heaters.

CPSCMay 13, 2009Nationwide• Polaris Industries Inc., of Medina, Minn.

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.

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FDAMay 13, 2009Nationwide• Computerized Medical Systems Inc

Philips Healthcare Inc.: Philips Avalon Fetal Monitor FM20; Model Number: M2702A.

Interruption of power-up/boot sequence may cause the paper scale and recorder speed settings of the monitor to revert to factory default may lead to misinterpretation of the fetal trace by the user and to potential incorrect clinical decisions

FDAMay 12, 2009Nationwide• Philips Healthcare Inc.

Steris Corp: Cmax 110v Surgical Table Hand Control. The Cmax Surgical...

A limited quantity of the Cmax Hand Controls, P150832-500, were manufactured without Loctite thread locker on the screws that attach the mounting clip to the hand control case. This clip provides a means of storing the hand control on the table side rails. It is possible that screws without Loctite can work loose and the clip can become separated from the hand control. If both screws back out c

FDAMay 12, 2009AL, AR, CA +34 more• Steris Corp

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...

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

Botanika Candles (DayNa Decker) – Fire Risk (2009)

Fire/Burn Risk

The recalled candles were sold under the DayNa Decker "Botanika" brand in 16-ounce green glass vessels, 4 inches wide by 5 inches high. Botanika candles in the smaller 3-ounce and 6-ounce sizes are not included in the recall. The words "DayNa Decker" and "Bacara," "Bardou," "Clementine," "Indigo," "Leila," "Manzanita," "Sierra," "Violetta," "Yasmin" or "Zelia" appear on the bottom of the glass vessel.

CPSCMay 12, 2009Nationwide• Southern California Candle Co. Inc., of Los Angeles, Calif.

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

GE Healthcare, LLC: Signa Excite" 1.5 T Magnetic Resonance Systems, manufactu...

Signa MR Excite" 1.5T system containing 11.1_M4_0818.a software, associated with 2D Fast Spin Echo based pulse sequences (2D FSE-XL, 2D FRFSE-XL, 2D FSE-IR, 2D T2FLAIR and 2D T1FLAIR) may experience an image flip along the phase encode direction and incorrect annotation, which may result in incorrect localization of anatomy in oblique axial images with the pulse sequences.

FDAMay 11, 2009AK, VT, WY +1 more• GE Healthcare, LLC

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

Arrow International Inc: 12 French 3 Lumen 16 cm Large-Bore Central Venous Cathete...

Wire guide can have difficulty passing through catheter juncture hub or being removed from the catheter.

FDAMay 8, 2009Nationwide• Arrow International Inc

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.

Arrow International Inc: 12 French 3 Lumen 20 cm Large-Bore Central Venous Cathete...

Wire guide can have difficulty passing through catheter juncture hub or being removed from the catheter.

FDAMay 8, 2009Nationwide• Arrow International Inc

Baxter Healthcare Corp. Rt.: Baxter Colleague CX Infusion Pump, Single Channel Volumet...

There was no documentation to show the required tests were performed following the replacement of the battery and battery harness.

FDAMay 8, 2009PR• Baxter Healthcare Corp. Rt.

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

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.