Kendall Kerlix Large Roll, 4.5 in X 4.1 yd, Sterile Product Number: 6730
FDA device recall Z-0381-04 · posted 2004-07-20 · Terminated
Recall details
- Recalling firm
- Kendall Healthcare Products Co
- Reason for recall
- Sterility compromised due to lack of package seal integrity
- Action taken
- 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
- Status
- Terminated
- Product code
- NAD
- Quantity affected
- 188 cases
- Distribution
- 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.
- Date initiated
- 2004-01-08
- Date posted
- 2004-07-20
- Date terminated
- 2012-05-15
- Location
- Mansfield, MA
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