MAQUET Inc. HANAULUX 2005 IXL cupola, P/N: 56076869. Intended to provide visible illumination for the surgical field or for the examination of the patient. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
HANAULUX 2005 IXL cupola, P/N: 56076869. Intended to provide visible illumination for the surgical field or for the examination of the patient.
Brand
MAQUET Inc.
Lot Codes / Batch Numbers
Part Number: 56076869, all serial numbers
Products Sold
Part Number: 56076869, all serial numbers
MAQUET Inc. is recalling HANAULUX 2005 IXL cupola, P/N: 56076869. Intended to provide visible illumination for the surgical due to Several reports have been received regarding one model of spring arm (Acrobat 200 series) in combination with surgical light from various Manufacturer. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Several reports have been received regarding one model of spring arm (Acrobat 200 series) in combination with surgical light from various Manufacturers. All incidents pertain to a crack on the front joint of the Acrobat arm.
Recommended Action
Per FDA guidance
Urgent Device Correction letters, dated October 7, 2009, were sent out by FedEx. The letter identified the affected products and asked customers to call 1-888-627-8383 #1, if they have any questions. The letter also provided a Technical Description along with a Customer Fax Response form. The letter stated the potential hazard and recommended precaution. If customers need additional info or have any questions they should contact their local MAQUET representative.
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