RecallDepth

Pre-filled Water Syringe, Model Numbers SW-010-100 and SW-010

This recall is currently active, issued June 5, 2025. It was issued by Healthmark Industries Co., Inc..

Company
Healthmark Industries Co., Inc.
Recall Initiated
May 2, 2025
Posted
June 5, 2025
Recall Number
Z-1909-2025
Quantity
250000 units
Firm Location
Fraser, MI
Official Source
View on FDA website ↗

Reason for Recall

During endoscope surveillance monitoring, a user facility identified contamination from duodenoscope samples that were linked to the Pre-filled Water Syringes as part of their investigation. Healthmark Industries conducted its own investigation and concluded that the Pre-filled Water Syringe had been improperly used outside of the intended purpose.

Distribution

US Nationwide and Internationally to countries of: Canada, Malaysia.

Lot / Code Info

Lot Numbers: 200001 200002 200003 200004 200005 200006 200007 200008 200009 200010 200011 200012 200013

Root Cause

Under Investigation by firm

Action Taken

An "URGENT PRODUCT RECALL" notification letter was sent to customers beginning 5/2/25. Recommended Mitigations/ User Recommendations Please discontinue use of the Pre-Filled Water Syringes containing non-sterile water, which can be identified by a red cap. Any unused product can be returned for credit or replacement. Customer are requested to take the following actions 1. Ensure all affected product in your facility s inventory is no longer in use and has been properly quarantined. 2. Please ensure this message is forwarded to any individuals that need notification within your organization or any organization where the affected products have been transferred. 3. Contact Customer Service via email at HMCS@hmark.com or 800-521-6224 to return your unused affected product or if you have any questions. 4. Complete and return the response form Getinge by e-mailing a copy to recallresponses.qrc@getinge.com.

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