Recall Z-0962-2020— Cook Inc.
Class II · Terminated
Class II FDA medical device recall by Cook Inc., initiated 2019-01-04, terminated 2020-05-29. It names one FDA 510(k) clearance: K082536. Product: PTFE Wire Guide, Guidewire, Global Product Number 638813 635413-10. Reason: The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip..
- Recalling firm
- Cook Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-01-04
- Terminated
- 2020-05-29
- Firm location
- Bloomington, IN, United States
510(k) clearances named in this recall
1 on FDA's recordK-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.
Product description
PTFE Wire Guide, Guidewire, Global Product Number 638813 635413-10
Reason for recall
The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip.
Data sourced from openFDA. This site is unofficial and independent of the FDA.