Recall Z-0381-04 ยท NAD Dressing, Wound, Occlusive
Kendall Healthcare Products Co
Kendall Kerlix Large Roll, 4.5 in X 4.1 yd, Sterile Product Number: 6730
| Date | Jul 20, 2004 (initiated Jan 8, 2004) |
| Status | Terminated |
| Reason | Sterility compromised due to lack of package seal integrity |
| Root cause | Other |
| Action | Kendall issued Recall letters by US Mail to all customers on January 8, 2004, requesting product be returne and dealer customers be notified. |
| Quantity | 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. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.