Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:29564
Brand Name:VASER Amplifiers and accessories
Model:
Affected:All serial numbers
Software version:
Recalling Organisation:Bausch & Lomb (NZ) Ltd
c/o Corporate services New Zealand
Level 5, 79 Queen Street
Auckland 1010
Contact Information:
Manufacturer:Solta Medical Inc
Issue:The current User Manual does not contain information on potential undesirable side effects that may be caused when not properly using the device. It is advised that the end user of this device is the licensed physicians, who are well trained and well aware of the potential AE if the device is not used properly.
Recall action type:Correction
Recall action:Instructions for use to be updated
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:16/6/2022
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