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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

Class I (Serious)

Most Recent

Nov 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 2241–2260 of 2399 recalls

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.

1...111 112113114 115...120

Page 113 of 120Next

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

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

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

Xoran Technologies, Inc.: Xoran MiniCAT System for ENT (server and work station), ...

Misbranding; These devices do not bear the manufacturer's name or address.

FDAJan 4, 2008Nationwide• Xoran Technologies, Inc.

Rockwell Medical Technologies, Inc: RenalPure Liquid Acid Concentrate R-006; One Gallon (3.78...

Foil Seal Deterioration; occuring on the tamper resistant foil seals on dialysis liquid concentrate and Dri-Sate product containers older than two years old.

FDADec 3, 2007Nationwide• Rockwell Medical Technologies, Inc

Rockwell Medical Technologies, Inc: Glacial Acidic Acid (liquid component of Dri-Sate Dry Ac...

Foil Seal Deterioration; occuring on the tamper resistant foil seals on dialysis liquid concentrate and Dri-Sate product containers older than two years old.

FDADec 3, 2007Nationwide• Rockwell Medical Technologies, Inc

Rockwell Medical Technologies, Inc: Dri-Sate Glacial Acidic Acid (liquid component of Dri-Sat...

Foil Seal Deterioration; occuring on the tamper resistant foil seals on dialysis liquid concentrate and Dri-Sate product containers older than two years old.

FDADec 3, 2007Nationwide• Rockwell Medical Technologies, Inc

Sechrist Industries Inc: Sechrist Hyperbaric Chamber Gurney, Standard Gurney & St...

Brake Problems: The stretcher brake cams may crack while attempting to lock the stretcher brake (Sechrist is supplied the stretchers by the manufacturer Stryker Medical)

FDAOct 31, 2007Nationwide• Sechrist Industries Inc

Fertility Technology Resources, Inc.: Tucker Embryo Catheter with URM Tip, Embryo Transfer Cath...

Expiration Date for sterility; The 5 year dating could not be validated/supported for sterility assurance.

FDASep 13, 2007CA, CO, FL +13 more• Fertility Technology Resources, Inc.

Fertility Technology Resources, Inc.: Tucker Embryo Catheter, Stylet, For use with Embryo Trans...

Expiration Date for Sterility; The 5 year dating could not be validated/supported for sterility assurance.

FDASep 13, 2007CA, CO, FL +13 more• Fertility Technology Resources, Inc.

Fertility Technology Resources, Inc.: Tucker Embryo Catheter for Trial Transfer, 20 cm, Order #...

Expiration Date for sterility; The 5 year dating could not be validated/supported for sterility assurance.

FDASep 13, 2007CA, CO, FL +13 more• Fertility Technology Resources, Inc.

Fertility Technology Resources, Inc.: Morton IUI Catheter, Sterile, Single Use Only, Order #: f...

Expiration Date for sterility; The 5 year dating could not be validated/supported for sterility assurance.

FDASep 13, 2007CA, CO, FL +13 more• Fertility Technology Resources, Inc.

Inotech Biosystems Intl., Inc: Inotech brand Heparin Adsorbant, Catalog #: HA-1, in 10m...

Erroneous Coagulation Tests

FDAAug 20, 2007Nationwide• Inotech Biosystems Intl., Inc

VNUS Medical Technologies Inc: VNUS 7F ClosureFAST Catheter, Order #: CF7-7-60 (60 cm wo...

Instructions for Use change: Instructions for Use have been changed to include a modified placement recommendation.

FDAAug 8, 2007Nationwide• VNUS Medical Technologies Inc

Hitachi Medical Systems America Inc: Altaire Shoulder Coil, an accessory to the Altaire MRI sy...

Overheating; A portion (balun assembly) of the cable that connects the shoulder coil to the actual MRI unit may malfunction and result in overheating of the balun assembly. The overheating of the balun assembly could result in injury to the patient or operator if either came into contact with the assembly.

FDAJul 30, 2007Nationwide• Hitachi Medical Systems America Inc

EMD Chemicals Inc: Harleco May and Grunwald's Stain; 0.17% w/v; Methanol Sol...

Out of Spec -- The Batch (Lot) was incorrectly released after being rejected for out of specification of high azure and eosin absorbance at the end of the run and particulate matter at the end of the run.

FDAJul 30, 2007IN• EMD Chemicals Inc

Wallach Surgical Devices, Inc.: Wallach Cryotip T-00337 Anorectal Tip used with the Cryos...

The tip may separate from the probe.

FDAJun 6, 2007Nationwide• Wallach Surgical Devices, Inc.

Roche Molecular Systems, Inc.: Amplilink Software versions 1.1, 1.3, 1.4, 2.41. COBAS Am...

For select COBAS AMPLICOR Tests run on the COBAS AMPLICOR Analyzer in conjunction with AMPLILINK software, a discrepancy has been identified between the onboard working reagent stability information reported by AMPLILINK Software (versions 1.1, 1.3, 1.4 and 2.41) and the stability information provided in the test kit package inserts/method manual.

FDAMay 21, 2007Nationwide• Roche Molecular Systems, Inc.