Ultracell Ear Wick Fenestrated 9mm DIA x 15mm Catalog #: 30305-C
FDA Recall Z-0482-03 · Posted 2003-01-30
Recalling FirmUltracell Medical Technologies
Recall StatusTerminated
Product CodeKCN
Date Initiated2003-01-08
Date Terminated2012-05-01
Product Quantity33 boxes
Reason for Recall
Sterility of the device is compromised
Firm Action
Ultracell Medical Technologies initiated the recall by fax or mail on 1/8/03. The firm requested return of product . Distributors were requestd to recall to their accounts.
Root Cause
Other
Distribution Pattern
Nationwide
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.