Kendall Kerlix Large Roll, 4.5 in X 4.1 yd, Sterile Product Number: 6730
FDA Recall Z-0381-04 · Posted 2004-07-20
Recalling FirmKendall Healthcare Products Co
Recall StatusTerminated
Product CodeNAD
Date Initiated2004-01-08
Date Terminated2012-05-15
Product Quantity188 cases
Reason for Recall
Sterility compromised due to lack of package seal integrity
Firm Action
Kendall issued Recall letters by US Mail to all customers on January 8, 2004, requesting product be returne and dealer customers be notified.
Root Cause
Other
Distribution Pattern
AL, AZ, CA, CO, FL, GA, IL, KY, LA, MA, MD, MN, MO,NC NE, NJ, NY, OH, PA, RI, TN, TX, VA, WA, WI, WV.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.