Ascent Healthcare Solutions, Inc. Tourniquet Cuff Single Port Single Bladder - Reprocessed Sterile device -- Pneumatic tourniquet. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Tourniquet Cuff Single Port Single Bladder - Reprocessed Sterile device -- Pneumatic tourniquet.
Brand
Ascent Healthcare Solutions, Inc.
Lot Codes / Batch Numbers
Catalog No 60-7075-003, Lot No 136548
Products Sold
Catalog No 60-7075-003, Lot No 136548
Ascent Healthcare Solutions, Inc. is recalling Tourniquet Cuff Single Port Single Bladder - Reprocessed Sterile device -- Pneumatic tourniquet. due to Sterility Compromised -- Ascent Healthcare Solutions cannot validate the sterilization process for a variety of Ascent Healthcare Solutions products.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sterility Compromised -- Ascent Healthcare Solutions cannot validate the sterilization process for a variety of Ascent Healthcare Solutions products.
Recommended Action
Per FDA guidance
A recall notification letter titled Voluntary Medical Device Recall was sent to each consignee. If you have questions about this recall on numerous reprocessed devices, contact Moira Barton-Varty at 888-888-3433, ext. 5350 or at mbarton@ascenths.com.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026