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Ascent Healthcare Solutions, Inc.

Ascent Healthcare Solutions, Inc. Recalls

All product recalls associated with Ascent Healthcare Solutions, Inc..

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Recall Summary

Total Recalls

1000

Past Year

593

Class I (Serious)

65

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 9501–9520 of 10391 recalls

Ascent Healthcare Solutions, Inc.: Mitek Angled Side Effect Electrode - Reprocessed Sterile ...

Sterility Compromised -- Ascent Healthcare Solutions cannot validate the sterilization process for a variety of Ascent Healthcare Solutions products.

FDAMar 11, 2008Nationwide• Ascent Healthcare Solutions, Inc.

Ascent Healthcare Solutions, Inc.: Kendall Calf Garment - Reprocessed Sterile device used to...

Sterility Compromised -- Ascent Healthcare Solutions cannot validate the sterilization process for a variety of Ascent Healthcare Solutions products.

FDAMar 11, 2008Nationwide• Ascent Healthcare Solutions, Inc.

Ascent Healthcare Solutions, Inc.: Zimmer Tourniquet Cuff - Reprocessed Sterile device -- P...

Sterility Compromised -- Ascent Healthcare Solutions cannot validate the sterilization process for a variety of Ascent Healthcare Solutions products.

1...474 475476477 478...520

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FDAMar 11, 2008Nationwide• Ascent Healthcare Solutions, Inc.

Ascent Healthcare Solutions, Inc.: Adult 02 Transducer (Nellcor) - Reprocessed Sterile devic...

Sterility Compromised -- Ascent Healthcare Solutions cannot validate the sterilization process for a variety of Ascent Healthcare Solutions products.

FDAMar 11, 2008Nationwide• Ascent Healthcare Solutions, Inc.

Ascent Healthcare Solutions, Inc.: Infant 02 Transducer (Nellcor) - Reprocessed Sterile devi...

Sterility Compromised -- Ascent Healthcare Solutions cannot validate the sterilization process for a variety of Ascent Healthcare Solutions products.

FDAMar 11, 2008Nationwide• Ascent Healthcare Solutions, Inc.

Ascent Healthcare Solutions, Inc.: Huntleigh Healthcare, Calf Garment - Regular. -- Reproces...

Sterility Compromised -- Ascent Healthcare Solutions cannot validate the sterilization process for a variety of Ascent Healthcare Solutions products.

FDAMar 11, 2008Nationwide• Ascent Healthcare Solutions, Inc.

Ascent Healthcare Solutions, Inc.: Zimmer, 34" Tourniquet Cuff Single Port Single Bladder Lu...

Sterility Compromised -- Ascent Healthcare Solutions cannot validate the sterilization process for a variety of Ascent Healthcare Solutions products.

FDAMar 11, 2008Nationwide• Ascent Healthcare Solutions, Inc.

Ascent Healthcare Solutions, Inc.: Arthrocare 3.6 mm Right Angle - Reprocessed Sterile devi...

Sterility Compromised -- Ascent Healthcare Solutions cannot validate the sterilization process for a variety of Ascent Healthcare Solutions products.

FDAMar 11, 2008Nationwide• Ascent Healthcare Solutions, Inc.

Ascent Healthcare Solutions, Inc.: Huntleigh Healthcare Thigh Garment. - Reprocessed Sterile...

Sterility Compromised -- Ascent Healthcare Solutions cannot validate the sterilization process for a variety of Ascent Healthcare Solutions products.

FDAMar 11, 2008Nationwide• Ascent Healthcare Solutions, Inc.

Ascent Healthcare Solutions, Inc.: Mitek 3.5 mm Side Effect Electrode - - Reprocessed Steril...

Sterility Compromised -- Ascent Healthcare Solutions cannot validate the sterilization process for a variety of Ascent Healthcare Solutions products.

FDAMar 11, 2008Nationwide• Ascent Healthcare Solutions, Inc.

Philips Medical Systems North America Co. Phillips: EasyVision RAD - Radiological Image Processor, software v...

Inaccurate measurements when exporting radiography images to Picture Archiving and Communication System (PACS ).

FDAMar 10, 2008Nationwide• Philips Medical Systems North America Co. Phillips

GE Healthcare: DST-XL Model 1002375 is a multi-head, whole body gamma ca...

GE Healthcare has recently became aware of a cable failure associated with the arm or gantry rotation of the DST-XL Camera that may impact patient safety.

FDAMar 10, 2008AL, AR, CA +21 more• GE Healthcare

GE Healthcare: GE Healthcare Definium 8000 Digital Radiographic System.

Radiation dose reading greater than actual dose: Error in the generator software on the GE Healthcare Revolution XR/d configured with HP 8200 PC consoles and all Definium 8000 systems may impact patient safety. Occasional generator software errors may cause light X-ray Images with reported mAs readings higher than was actually exposed to the patient using the overhead X-ray tube. The mAs rea

FDAMar 7, 2008Nationwide• GE Healthcare

GE Healthcare: GE Healthcare Definium 8000 Digital Radiographic System. ...

Loss of image data: Software anomaly in the Processing Software on the Definium 8000 system may impact patient safety when using the VolumeRAD advanced application (option). The slice visualization of VolumeRAD exams acquired on the Wallstand receptor will be offset by 17mm. This prevents the visualization of anatomy WITHIN a distance of 17mm from the wallstand patient barrier (receptor cover).

FDAMar 7, 2008Nationwide• GE Healthcare

Cardinal Health 303 Inc DBA Alaris Products: U19 Socketed Integrated Circuit ("U19 IC") on the logic b...

A channel error on an affected Alaris System module will stop an active infusion (or monitoring) with an audible and visual alarm. Channel errors due to failures of the U19 Socketed Integrated Circuits (U19 IC) on the logic board of the Alaris Pump module ("Pump module"). The user will be required to replace the affected module.

FDAMar 5, 2008AZ, AR, CA +37 more• Cardinal Health 303 Inc DBA Alaris Products

Cardinal Health 303 Inc DBA Alaris Products: U9 Socket Integrated Circuit ("U9 IC") on the display boa...

A channel error on an affected Alaris System module will stop an active infusion (or monitoring) with an audible and visual alarm. Channel errors due to failure of the U9 Socketed Integrated Circuits (U9 IC) on the display board of the Alaris Syringe Module ("Syringe module") and Alaris PCA module ("PCA module") for modules manufactured on or before October 4, 2005. The user will be required to re

FDAMar 5, 2008AZ, AR, CA +37 more• Cardinal Health 303 Inc DBA Alaris Products

Cardinal Health 303 Inc DBA Alaris Products: Grey Inter-Unit Interface Connectors ("IUI") on the follo...

A channel error on an affected Alaris System module will stop an active infusion (or monitoring) with an audible and visual alarm. Channel errors with the Alaris System due to the Inter-Unit Interface (IUI) connectors on all Alaris System modules (manufactured on or before March 26, 2004). Grey Inter-Unit Interface Connectors ("IUI") on the following Alaris System modules built on or before March

FDAMar 5, 2008AZ, AR, CA +37 more• Cardinal Health 303 Inc DBA Alaris Products

Baxter Healthcare Corp. Rt.: Baxter HEP LOCK (Heparin Lock Flush Solution, USP) 10 u/m...

Due to an increase of adverse events in Baxter single and multi-dose Heparin for injection products, which used the same active pharmaceutical ingredient (API) source as the HEP LOCK products

FDAFeb 28, 2008PR• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter HEP-LOCK (Preservative-Free Heparin Lock Flush Sol...

Due to an increase of adverse events in Baxter single and multi-dose Heparin for injection products, which used the same active pharmaceutical ingredient (API) source as the HEP LOCK products

FDAFeb 28, 2008PR• Baxter Healthcare Corp. Rt.

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

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