Comprehensive Shoulder System Mini Humeral Stem 9mm recall
Comprehensive Shoulder System Mini Humeral Stem 9mm,, Model No. 113629 - Product Usage: The intended use of the comprehensive humeral stem mini is to…
Why was Comprehensive Shoulder System Mini Humeral Stem 9mm recalled?
A 15mm Shoulder Mini Humeral Stem was misidentified as a 9mm Shoulder Mini Humeral Stem.
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 No. 659260, UDI Number: (1)00880304462649(17)290814(10)659260
- Product
- Comprehensive Shoulder System Mini Humeral Stem 9mm,, Model No. 113629 - Product Usage: The intended use of the comprehensive humeral stem mini is to…
- Recalling firm
- Biomet, Inc.
- Quantity
- 14 units
- Distribution
- International distribution in the countries of Canada, Japan, Netherlands, South Korea.
- Recall date
- April 1, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)