GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories
Reported: February 22, 2017 Initiated: January 9, 2017 #Z-1218-2017
Product Description
GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories
Reason for Recall
Generators may have a faulty component which could impact the proper functioning of the device.
Details
- Recalling Firm
- Aesculap Implant Systems LLC
- Units Affected
- 24 generators
- Distribution
- USA (nationwide Distribution).
- Location
- Center Valley, PA
Frequently Asked Questions
What product was recalled? ▼
GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories. Recalled by Aesculap Implant Systems LLC. Units affected: 24 generators.
Why was this product recalled? ▼
Generators may have a faulty component which could impact the proper functioning of the device.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 22, 2017. Severity: Moderate. Recall number: Z-1218-2017.
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