Recall Z-2717-2014— KCI USA, Inc.
Class II · Terminated
Class II FDA medical device recall by KCI USA, Inc., initiated 2014-05-19, terminated 2015-09-18. FDA's recall record names no specific 510(k) clearance for this event. Product: CelluTome Epidermal Harvesting System Part number CT-H25 or Part Number CT-H50. Reason: Blade can shift during shipping which makes the product ineffective..
- Recalling firm
- KCI USA, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-05-19
- Terminated
- 2015-09-18
- Firm location
- San Antonio, TX, United States
Product description
CelluTome Epidermal Harvesting System Part number CT-H25 or Part Number CT-H50
Reason for recall
Blade can shift during shipping which makes the product ineffective.
Data sourced from openFDA. This site is unofficial and independent of the FDA.