Arrow central venous catheterization kit, 14 ga x 20 cm
FDA device recall Z-0083-04 · posted 2003-11-01 · Terminated
Recall details
- Recalling firm
- Arrow International Inc
- Reason for recall
- wrong product in box
- Action taken
- 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.
- Root cause
- Other
- Status
- Terminated
- Product code
- KZH
- Quantity affected
- 240 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,
- Date initiated
- 2003-09-16
- Date posted
- 2003-11-01
- Date terminated
- 2004-04-05
- Location
- Reading, PA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| [CENTRAL VENOUS][MULTI-LUMEN] CATHETER W/FLEX TIP (K862056) | Arrow Intl., Inc. | 1986-08-25 |