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.
Take action
Contact the company
📍Recalling firmAtrium Medical Corporation40 Continental Blvd · Merrimack, NH 03054-4332
“Atrium Oasis Drain Single W/AC Recall: Shortened Expiration Date Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/56967-atrium-oasis-drain-single-w-ac-recall-shortened-expiration-date. Based on FDA recall #Z-0621-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0621-2024%22&limit=1).
Atrium Medical Corporation, with FDA approval, is recalling Atrium Oasis Drain Single W / AC (Part No. 3600-100) due to a sterilization nonconformance that inaccurately aged the product. The Food and Drug Administration announced this Class II recall on November 1, 2023.
How to tell if you have it
Brand: Atrium Medical
Product: Atrium Oasis Drain Single W / AC
Part No.: 3600-100
UDI-DI: 00650862110012
Lot codes: 492065 and 492075
The hazard
The sterilization nonconformance prematurely aged the product by 48.3 days, resulting in an inaccurate expiration date on the label. This creates an increased risk to patients and healthcare providers using the product after the shortened expiration date of November 17, 2025.
Context
GovInfoNow's records show Atrium Medical Corporation has 16 other recalls on record since November 22, 2017. Recent brand recalls include a September 9, 2024 iCast Stent recall for UDI label errors and a May 3, 2024 ADVANTA VXT Vascular Graft recall for slider separation risks. Other recent recalls of similar products include Cook Medical Multipurpose Drainage Catheter (March 5, 2026), Spectrum Central Venous Tray (March 5, 2026), and Arterial Pressure Tray (March 5, 2026).
How to tell if you have this one
Check for the product name 'Atrium Oasis Drain Single W/AC', part number 3600-100, and lot numbers 492065 or 492075. The expiration date on the label may be inaccurate, showing November 17, 2025.
Brand
Atrium Medical
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Expiration Date
Verify the expiration date on the label; if it shows November 17, 2025 or earlier, the product is recalled.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Domestic distribution nationwide. No foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0621-2024 (November 1, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0621-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.