Baxter Healthcare Corporation Recall 90032
Description: APD Drain Manifold
Baxter Healthcare Corporation Recall 90032 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | Z-1146-2022 |
| Event ID | 90032 |
| Event Description | APD Drain Manifold |
| Product Type | Devices |
| Distribution | US Nationwide distribution in the states of CA, MO, MA, AZ, TX, FL, NY, MD, OH. |
| Quantity | 180 units |
| Recall Reason | Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error. |
| Device Classification | 20220608 |
| Device Code Info | Product code: R5C4512; UDI: 00085412008790; Lot Number: H18D03030 (exp. date: 04/03/2023), Lot Number: H18E31046 (exp. date: 05/31/2023), Lot Number: H18L04065 (exp. date:12/04/2023), Lot Number: H20H10073 (exp. date: 08/10/2022) |
| Center Classification Date | 20220527 |
| Recall Initiation Date | 20220421 |
| Recalling Firm | Baxter Healthcare Corporation |
| Initial Notification | Letter |
| Similar To |