Aesculap Implant Systems LLC For intraventricular indications mainly used for operations within the brain ventricles. Product Code: FF399R Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
For intraventricular indications mainly used for operations within the brain ventricles. Product Code: FF399R
Brand
Aesculap Implant Systems LLC
Lot Codes / Batch Numbers
UDI-DI: 04038653065547 Lot Numbers: 52750146 52753381, 52756472, 52768317, 52805655, 52812596, 52816570, 52823878, 52830872. Serial Numbers: 4281, 4282, 4284, 4288, 4289, 4291, 4308, 4309, 4310, 4312, 4313, 4336, 4340, 4341, 4342, 4402, 4411, 4412, 4413, 4414, 4422, 4439, 4447, 4449, 4450
Products Sold
UDI-DI: 04038653065547 Lot Numbers: 52750146 52753381, 52756472, 52768317, 52805655, 52812596, 52816570, 52823878, 52830872. Serial Numbers: 4281,4282, 4284,4288, 4289,4291, 4308,4309, 4310, 4312, 4313,4336, 4340,4341, 4342,4402, 4411, 4412, 4413,4414, 4422,4439, 4447,4449, 4450
Aesculap Implant Systems LLC is recalling For intraventricular indications mainly used for operations within the brain ventricles. Product Cod due to Trocar manufactured with the shaft too long and does not meet manufacturing specifications. As a result, when used with the 30 neuroendoscope, a porti. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Trocar manufactured with the shaft too long and does not meet manufacturing specifications. As a result, when used with the 30 neuroendoscope, a portion of the visual field is obscured.
Recommended Action
Per FDA guidance
Aesculap issued Urgent Medical Device Recall Notification Letter via USPS Certified Mail 20.JUL.2023. Letter states reason for recall, health risk and action to take: 1. Review the Recall Notification in its entirety and ensure that all users in your organization of the above-mentioned product, and all concerned persons are informed about this voluntary product recall. 2. Your Aesculap Sales Representative will be in contact with you to review your current inventory, aid in evaluating your devices and assist you in completing the attached Product Acknowledgement Form. 3. Do not destroy any affected product. 4. Utilizing the attached form, you and your Sales Representative will record the total number of individual impacted pieces. If you have no inventory remaining, a zero (0) will be entered on the form. 5. Return the completed "Product Acknowledgement Form" to Aesculap, Inc. Product Quality Excellence department by emailing the form to PA_QualityAssurance.BBMUS_Service@bbraunusa.com or faxing the form to (610) 849-1197 after your inventory has been evaluated by your Sales Representative, even if the total inventory in your possession is zero (0). 6. Once Aesculap, Inc. receives your "Product Acknowledgement Form", a customer support representative will contact you with instructions on how to return any impacted pieces in your possession.
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