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Biomet Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 12 MM, 83 MM Long Item Number: 113632 - safety alert
Official notice
2 Mar 2022
Last checked
2 Mar 2022
An official FDA notice concerns Biomet Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 12 MM, 83 MM Long Item Number: 113632 - safety alert. An official FDA notice concerns Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 12 MM, 83 MM Long Item Number: 113632. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2022-03-02. Lots: 327160. Recall numbers: Z-0675-2022. Check the official notice for the complete list. Published 2022-03-02.
What to do now
The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.
Units affected
12
Recall number
Z-0675-2022
Official notice
2022-03-02
The hazard
The hazard
An official FDA notice concerns Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 12 MM, 83 MM Long Item Number: 113632. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2022-03-02. Lots: 327160. Recall numbers: Z-0675-2022. Check the official notice for the complete list.
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
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Affected products
Product 1
Units affected
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Affected area 2
Company & contacts
Company & contacts
Brand: Biomet. Contact: Biomet, Inc..
Source & status
Source & status
Recall details
Recall details
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Event id
Units affected
Status
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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