LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120
Reported: July 31, 2019 Initiated: June 18, 2019 #Z-2057-2019
Product Description
LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120
Reason for Recall
The products' cut, coagulate, or blend function may not operate with the use of the Foot Pedal.
Details
- Recalling Firm
- CooperSurgical, Inc.
- Units Affected
- 358
- Distribution
- Nationwide domestic distribution. International distribution to Canada and Costa Rica.
- Location
- Trumbull, CT
Frequently Asked Questions
What product was recalled? ▼
LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120. Recalled by CooperSurgical, Inc.. Units affected: 358.
Why was this product recalled? ▼
The products' cut, coagulate, or blend function may not operate with the use of the Foot Pedal.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 31, 2019. Severity: Moderate. Recall number: Z-2057-2019.
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