BIOMET 3i LOW PROFILE ABUTMENT NON-HEXED PREFORMANCE recall
BIOMET 3i LOW PROFILE ABUTMENT NON-HEXED PREFORMANCE TEMPORARY CYLINDER An endosseous dental implant abutment is a premanufactured prosthetic…
Why was BIOMET 3i LOW PROFILE ABUTMENT NON-HEXED PREFORMANCE recalled?
A limited number of product pouches may not have been sealed during packaging.
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?
Part #LPCPTC2 Lot #'s 2016011174, 2016011175 and 2016011178
- Product
- BIOMET 3i LOW PROFILE ABUTMENT NON-HEXED PREFORMANCE TEMPORARY CYLINDER An endosseous dental implant abutment is a premanufactured prosthetic…
- Recalling firm
- Biomet 3i, LLC
- Quantity
- 270
- Distribution
- Worldwide Distribution to Austria, Belgium, Switzerland, Germany, Spain, France, Great Britain, Ireland, Italy, Lithuania, Portugal and Sweden
- Recall date
- December 28, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)