FDAClass IIJuly 27, 2022

Universal Robot UR5 arm recall

Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010

Why was Universal Robot UR5 arm recalled?

Malfunction of the robotic arm preventing further movement of the robotic arm and requiring restart of the robotic digital microscope system.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI-DI: 04046955206742, Serial Number: SN1004

Product
Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010
Recalling firm
Aesculap Implant Systems LLC
Quantity
1
Distribution
United States: NE
Recall date
July 27, 2022
Classification
Class II
Status
Completed
Agency
FDA (device)
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