aap Implante AG recall
aap Implante AG, Lambotte chisel, 20 mm, REF IU 3000-20 Product Usage: Surgical instruments are intended to aid in the insertion of bone plates and…
Why was aap Implante AG recalled?
There is the potential for the Lambotte chisel to break at the welded piece parts of the chisel body and knocking plate.
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?
Lot Numbers: I011, I012, I013, I014, I015, I016, I017
- Product
- aap Implante AG, Lambotte chisel, 20 mm, REF IU 3000-20 Product Usage: Surgical instruments are intended to aid in the insertion of bone plates and…
- Recalling firm
- AAP Implantate Ag
- Quantity
- 25 units
- Distribution
- Worldwide Distribution - US Nationwide in the state of Texas and country of Germany
- Recall date
- March 27, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)