Endotrac EPF/EGR Push Blade, Catalog Number 3053-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.
Reported: September 4, 2019 Initiated: July 25, 2019 #Z-2416-2019
Product Description
Endotrac EPF/EGR Push Blade, Catalog Number 3053-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.
Reason for Recall
The seal integrity of the sterile bag containing the kits may be compromised.
Details
- Recalling Firm
- Stryker GmbH
- Units Affected
- 251
- Distribution
- US Nationwide Distribution
- Location
- Selzach, N/A
Frequently Asked Questions
What product was recalled? ▼
Endotrac EPF/EGR Push Blade, Catalog Number 3053-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.. Recalled by Stryker GmbH. Units affected: 251.
Why was this product recalled? ▼
The seal integrity of the sterile bag containing the kits may be compromised.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 4, 2019. Severity: Moderate. Recall number: Z-2416-2019.
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