MAQUET Inc. Kion Anesthesia Workstation Maquet Critical Care AB SE-171-95 Solna, Sweden Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Kion Anesthesia Workstation Maquet Critical Care AB SE-171-95 Solna, Sweden
Brand
MAQUET Inc.
Lot Codes / Batch Numbers
Article number 6454800 and 6462910 Serial # 1719, 2034, 3078, 3416, 3417, 3418, 3419, 3420, 3027.
Products Sold
Article number 6454800 and 6462910 Serial # 1719, 2034, 3078, 3416, 3417, 3418, 3419, 3420, 3027.
MAQUET Inc. is recalling Kion Anesthesia Workstation Maquet Critical Care AB SE-171-95 Solna, Sweden due to Overcharging of batteries and the release of acid fumes. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Overcharging of batteries and the release of acid fumes
Recommended Action
Per FDA guidance
Safety Alert letters were sent out by FedEx tracking. A Service Express letter will be sent out emphasizing that only qualified batteries must be used in KION equipment and will list all qualified battery types. A Field Action - update of existing operating manuals will include warning on battery charging on KION. This action is currently scheduled to start 9/1/07 and be completed in US by 10/1/07. After FDA consultation the recalling firm issued a 9/5/2007 URGENT DEVICE CORRECTION Letter stating that KION will visit consignees and replace batteries older than three years, verify that the batteries are ones of the approved type, and verify battery condition.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026