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Aesculap Implant Safil QUI + UNDY 5/0 (1) 45CM DSMP13 Suture - safety alert
Official notice
2 Nov 2016
Last checked
2 Nov 2016
An official FDA notice concerns Aesculap Implant Safil QUI + UNDY 5/0 (1) 45CM DSMP13 Suture - safety alert. An official FDA notice concerns Safil QUI + UNDY 5/0 (1) 45CM DSMP13 Suture. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2016-11-02. Lots: 115441. Recall numbers: Z-0316-2017. Check the official notice for the complete list. Published 2016-11-02.
What to do now
The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.
Units affected
180
Recall number
Z-0316-2017
Official notice
2016-11-02
The hazard
The hazard
An official FDA notice concerns Safil QUI + UNDY 5/0 (1) 45CM DSMP13 Suture. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2016-11-02. Lots: 115441. Recall numbers: Z-0316-2017. 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.
Lots
Event Ids
Recall Numbers
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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: Aesculap Implant. Contact: Aesculap Implant Systems LLC.
Source & status
Source & status
Recall details
Recall details
Recall number
Event id
Units affected
Status
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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