FLEXIBLE NEURO-FIBERSCOPE, 3.7MM X 34CM, Model # 11282BN1
Reported: September 4, 2019 Initiated: February 20, 2019 #Z-2425-2019
Product Description
FLEXIBLE NEURO-FIBERSCOPE, 3.7MM X 34CM, Model # 11282BN1
Reason for Recall
The action is being initiated due to Flexible Neuroscopes manufactured with the incorrect channel port.
Details
- Recalling Firm
- Karl Storz Endoscopy
- Units Affected
- 22 scopes
- Distribution
- US: FL, MO, MA, AL,CA, OH, PA,NH, OR, WA, MI, NC, CA, VA
- Location
- El Segundo, CA
Frequently Asked Questions
What product was recalled? ▼
FLEXIBLE NEURO-FIBERSCOPE, 3.7MM X 34CM, Model # 11282BN1. Recalled by Karl Storz Endoscopy. Units affected: 22 scopes.
Why was this product recalled? ▼
The action is being initiated due to Flexible Neuroscopes manufactured with the incorrect channel port.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 4, 2019. Severity: Moderate. Recall number: Z-2425-2019.
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