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Terminated

Dual Incu i, (Atom Infant Incubator Model 100) Atom Medical Corporation 3-18-15 Hongo, Bunkyo-Ku, Tokyo, Japan 113-0033 Usage: An incubator for infants.

FDA Recall Z-1945-2012 · Posted 2012-07-06

Recall StatusTerminated
Product CodeFMZ
Date Initiated2012-05-01
Date Terminated2013-01-31
Product Quantity377 units

Reason for Recall

There is a potential for the device's canopy to move unintentionally when using the incubator mode or radiant warmer mode.

Firm Action

Atom Medical sent an Urgent Field Safety Notice dated May 1, 2012, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to immediately identify all affected product in their inventory and quarantine them until the rework was complete. Customers were also asked to identify any customers to whom they further distributed the product and to contact their customers at once and arrange a time in whcih the filed service technician could perform the rework. Customers were asked to return the Recall Response Forms to Atom Medical ([email protected], [email protected], or [email protected]). All forms should be completed and returned by January 31, 2013. For questions regarding this recall call 512-327-9997.

Root Cause

Device Design

Distribution Pattern

Worldwide Distribution - USA including PA. Internationally to Japan, Kuwait, Saudi Arabia, Lenanon, Italy, Spain, China, East Europe, Slovakia, Poland, Czech Republic, Ukraine, Egypt, Russia, Algeria, Colombia, Germany, Malaysia, Switzerland, Australia, Europe, Portugal, Iran, Israel, Philippines, UAE, Korea, and Netherlands

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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