FDA Medical Device Recalls (openFDA)
Aesculap Inc: Aeos Robotic Digital Microscope, Product Code: PV010
- Recall number
- Z-2139-2024
- Recalling firm
- Aesculap Inc
- Product
- Aeos Robotic Digital Microscope, Product Code: PV010
- Status
- Open, Classified
- Initiated
- 2024-05-13
- Posted
- 2024-06-12
- Terminated
- not on file
- Reason
- Possibility of the robotic arm to drop more than 10cm from its original position after pressing the emergency stop button due to failure of the integrated safety mechanism.
- Root cause
- Process control
- Action
- On May 13, 2024, URGENT MEDICAL DEVICE FIELD CORRECTION letters were mailed to customers. Actions to be taken by the customer: 1. Review the Device Correction Notification in its entirety and ensure that all users in your organization of the device and other concerned persons are informed about this voluntary product correction. If you are a distributor, please forward this correction notification to your customers. The correction is to be extended to the end user/customer level. 2. Determine your current inventory of the affected material within your facility, cease use and quarantine product subject to correction. Do not destroy any affected product. (Once your completed Urgent Medical Device Form is received, a representative will be in contact to arrange for inspection and testing). 3. Utilizing the attached "Urgent Medical Device Correction Acknowledgement Form," record the total number of individual units in your posession. If you have no inventory, please enter zero (0) on the form. 4. Return the completed "Urgent Medical Device Correction Acknowledgement Form" to the Aesculap Inc. Quality Assurance Department by faxing the form to (610)849-1197 or e-mail to recalls@bbraunusa.com within two (2) weeks of receipt, even if the total inventory in your possession is zero (0). 5. Once we receive your acknowledgement Form, an Aesculap representative will contact you to arrange inspection and testing of your devices by our authorized specialists. Should you identify a problem or safety concern with the product, please report promptly by contacting our Post-market Surveillance Department at 1-833-425-1464. Additionally, adverse reactions of quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting Program wither online, by regular mail or fax.
- Quantity
- 19 units
- Distribution
- US Nationwide distribution in the states of AR, FL, IL, IN, KY, MI, NC, NE, OK, SD, TX.
- Lot, serial or model codes
- Product Code: PV010, UDI/DI: 04046955206742; Serial Numbers: 1011, 1005, 1057, 1032, 1038, 1054, 1036, 1060, 1056, 1089, 1093, 1027, 1061, 1004, 1026, 1035, 1097, 1084, 1063
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FSO
- Firm FEI
- 2916714
- Firm city
- Center Valley
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28