Biomet Comprehensive Reverse Shoulder Glenosphere Mini recall
Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate With Taper Adapter-indicated for primary, fracture, or revision total shoulder…
Why was Biomet Comprehensive Reverse Shoulder Glenosphere Mini recalled?
Package is intended to contain one (1) baseplate and one (1) taper adapter; however, devices may be packaged with two (2) baseplates and no (0) adapters.
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 Number: 410420 UDI: (01) 0 0880304 53246 5 (17) 290825 (10) 410420
- Product
- Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate With Taper Adapter-indicated for primary, fracture, or revision total shoulder…
- Recalling firm
- Biomet, Inc.
- Quantity
- 21 units
- Distribution
- International distribution - country of Netherland.s
- Recall date
- April 8, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)