APD Drain Manifold
Reported: June 8, 2022 Initiated: April 21, 2022 #Z-1146-2022
Product Description
APD Drain Manifold
Reason for Recall
Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.
Details
- Recalling Firm
- Baxter Healthcare Corporation
- Units Affected
- 180 units
- Distribution
- US Nationwide distribution in the states of CA, MO, MA, AZ, TX, FL, NY, MD, OH.
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
APD Drain Manifold. Recalled by Baxter Healthcare Corporation. Units affected: 180 units.
Why was this product recalled? ▼
Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 8, 2022. Severity: Moderate. Recall number: Z-1146-2022.
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