Z-1141-2022 Class II

Recalled by Baxter Healthcare Corporation — Deerfield, IL

Recall Details

Product Type
Devices
Report Date
June 8, 2022
Initiation Date
April 21, 2022
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
510 units

Product Description

15 Liters Drain Bag

Reason for Recall

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

Distribution Pattern

US Nationwide distribution in the states of CA, MO, MA, AZ, TX, FL, NY, MD, OH.

Code Information

Product code: R5C4145P; UDI: 05413760005386; Lot Numbers: H17H14104 (exp. date: 07/31/2022), H20K02117 (exp. date: 11/02/2025), H21H24081 (exp. date: 08/24/2026)