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Open, Classified

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

FDA Recall Z-0621-2024 · Posted 2023-12-28

Recall StatusOpen, Classified
Product CodeCAC
Date Initiated2023-11-01
Product Quantity835 cases total (6 units/case)

Reason for Recall

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.

Firm 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.

Root Cause

Nonconforming Material/Component

Distribution Pattern

Domestic distribution nationwide. No foreign distribution.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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