Ascent Healthcare Solutions, Inc. Zimmer, 34" Tourniquet Cuff Single Port Single Bladder Luer Lock Connector Brown Trim, Latex Free - Reprocessed Sterile device -- Pneumatic tourniquet. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Zimmer, 34" Tourniquet Cuff Single Port Single Bladder Luer Lock Connector Brown Trim, Latex Free - Reprocessed Sterile device -- Pneumatic tourniquet.
Brand
Ascent Healthcare Solutions, Inc.
Lot Codes / Batch Numbers
Cataloge No 60-7075-006, Lot No 115010
Products Sold
Cataloge No 60-7075-006, Lot No 115010
Ascent Healthcare Solutions, Inc. is recalling Zimmer, 34" Tourniquet Cuff Single Port Single Bladder Luer Lock Connector Brown Trim, Latex Free - 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