American Contract System Convenience Kits, CV B PACK, Model/Catalog Number: TNCB10AP
FDA Recall Z-3002-2026 · Posted 2026-08-21
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Recalling FirmAmerican Contract Systems Inc
Recall StatusOpen, Classified
Product CodeOEZ
Date Initiated2026-06-29
Product Quantity30 units
Reason for Recall
The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representative samples did not meet applicable performance specifications.
Firm Action
An URGENT: MEDICAL DEVICE RECALL NOTIFICATION letter dated 6/29/26 was sent to customers.
ACTIONS TO TAKE:
"Identify, segregate, and quarantine all impacted product. Other components within the convenience kits can still be used once kit is properly labeled with the warning label below.
"Add warning labels to affected ACS kits to ensure all users are aware of the actions below and identified in the enclosed Medline recall notice. A labeling template is enclosed for printing labels which can be affixed on all affected kits and cases in inventory. Please contact your Sales Representative if pre-printed labels are needed. This label should be applied in a prominently visible location to end-users. The location chosen should not cover any other critical product information found on existing product labeling.
"Customers (end-users): If you received product from a distributor, please contact the distributor or your sales representative with any questions you may have, or to request printed labels.
"Distributors: If any of the affected kits identified above were further distributed, please ensure all end-users are appropriately notified and maintain records of effectiveness.
"Complete the attached Recall Response Form and return by July 17, 2026.
Report any quality problems or adverse events associated with the products listed in this notification to [email protected] . Your assistance is appreciated and necessary to prevent any risk to patient or medical professional health as a result of not following these instructions.
Root Cause
Nonconforming Material/Component
Distribution Pattern
US Nationwide distribution in the states of IA, OH.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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