Modulift VBR Sz.m 4mm SET Screw Driver recall
MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441
Why was Modulift VBR Sz.m 4mm SET Screw Driver recalled?
Set screwdriver fails during surgery by deforming at the tip during engagement and manipulation of the implant.
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: 04046964067648
- Product
- MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441
- Recalling firm
- Aesculap Implant Systems LLC
- Quantity
- 9 pieces
- Distribution
- US: CA, FL, GA, IL, OH & MI
- Recall date
- July 27, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)