PlainRecalls
FDA Devices Moderate Class II Ongoing

Locking Cap for PD Catheter Adapter

Reported: June 8, 2022 Initiated: April 21, 2022 #Z-1142-2022

Product Description

Locking Cap for PD Catheter Adapter

Reason for Recall

Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.

Details

Units Affected
75 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?
Locking Cap for PD Catheter Adapter. Recalled by Baxter Healthcare Corporation. Units affected: 75 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-1142-2022.