FDA Recall Open, Classified

Atrium Oasis Drain Single W / AC, Part No. 3600-100

Recall: Z-0621-2024 · Initiated November 1, 2023

Recall

Recall Number
Z-0621-2024
Event Number
93553
Firm
Atrium Medical Corporation
FEI Number
3011175548
Product Code
CAC
Status
Open, Classified
Root Cause
Nonconforming Material/Component
Initiated
November 1, 2023
Posted
December 28, 2023
Address
40 Continental Blvd, Merrimack, NH, 03054-4332

Description

Atrium Oasis Drain Single W / AC, Part No. 3600-100

Reason

A sterilization nonconformance prematurely aged the product by 48.3 days, resulting in the expiration date on the label not being accurate. This nonconforming product was inadvertently distributed to customers. Increased risk to patients and healthcare providers using the product after the shortened expiration date of November 17, 2025.

Action

On November 1, 2023, the firm issued URGENT MEDICAL DEVICE - Removal letters to affected customers. Customers were instructed to remove any product from the affected lots from areas of use. Customers with affected product are entitled to a replacement at no cost to their facility. Customers will receive replacements upon their acknowledgement that they have affected product for return. Distributors should forward recall documentation to affected customers. Customers with questions may contact their Atrium/Getinge representative or call the Atrium/Getinge Customer Support at (603) 880-1433 (press option 1), Monday through Friday, 9AM-6PM Eastern Time Zone.

Distribution

Domestic distribution nationwide. No foreign distribution.

Quantity

835 cases total (6 units/case)