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Terminated

Micro Introducer Kit 5F, Model number: KIT-014-29, & Customer Model number: 7204. Vascular Solutions, 6464 Sycamore Court, Minneapolis, MN 53369.

FDA Recall Z-1592-2010 · Posted 2010-05-11

Recalling FirmGalt Medical Corp
Recall StatusTerminated
Product CodeDRE
Date Initiated2010-02-08
Date Terminated2011-03-21
Product Quantity400 units

Reason for Recall

Potential problem with pouch seal thus affecting sterile product.

Firm Action

Firm notified distributor by telephone 2/8/2010. Firm and distributor partnered to notify customers by an Urgent: Medical Device Recall - Lot Specific letter, dated 2/10/2010, beginning 2/16/2010. The letter identified the affected product and the reason for the recall. The letter asked customers to immediately check their inventory remove any affected kits and place them in a secure location. Customers are to complete the Product Recall Inventory Form and fax it to the Customer Service Department. Customers are also to contact Customer Service for a Return Authorization Number at 1-866-240-6001. Affected products will be replaced upon receipt. Questions or concerns should be directed to a local Sales Representative or Jill Eisenzimmer, Product Manager, at 763-656-4300.

Root Cause

Packaging process control

Distribution Pattern

Nationwide Distribution -- MI, PA, IL, & Washington, D.C.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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