Recall Z-0082-04 ยท KZH Introducer, Syringe Needle
Arrow International Inc
Arrow Howes multi-lumen central venous catheterization kit 7 Fr x 20 cm
| Date | Nov 1, 2003 (initiated Sep 16, 2003) |
| Status | Terminated |
| Reason | wrong product in box |
| Root cause | Other |
| Action | The recalling firm issued a recall letter to their direct customers dated 9/16/03. The recall letter explained the reason for recall and to return the product. |
| Quantity | 4480 units |
| Distribution | The products were shipped to distributors in AL, AZ, CA, CO, FL, HI, IL, IN, KS, MD, MI, MN, MO, NC, NM, NY, OH, PA, TN, TX, VA, and WI. The products were shipped to government accounts in AZ, AK, DC, IN, SC, and VA. The products were shipped to hospitals nationwide. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K900263 | ANTIMICROBIAL MULTI-LUMEN CENTRAL VENOUS CATHETER Arrow Intl., Inc., Jul 24, 1990 |