FDA Recall 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.

Recall: Z-1945-2012 · Initiated May 1, 2012

Recall

Recall Number
Z-1945-2012
Event Number
61807
Firm
Atom Medical Corporation 3-18-15 Hongo Bunkyo-Ku Japan
FEI Number
3005652389
Product Code
FMZ
Status
Terminated
Root Cause
Device Design
Initiated
May 1, 2012
Posted
July 6, 2012
Terminated
January 31, 2013

Description

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.

Reason

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

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.

Distribution

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

Quantity

377 units