CelluTome Epidermal Harvesting System Part number CT-H25 or Part… — Class II medical device recall Z-2717-2014
Terminated recall by KCI USA, Inc., reported 2014-10-08, distributed nationwide. Blade can shift during shipping which makes the product ineffective.
| Recall number | Z-2717-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | KCI USA, Inc., San Antonio, TX, United States |
| Recall initiated | 2014-05-19 |
| Classified | 2014-09-29 |
| Reported by FDA | 2014-10-08 |
| Terminated | 2015-09-18 |
| Distributed | Nationwide (US) |
| Quantity | 1,331 units |
| Lot numbers | 3244680000, 3245120000, 3245670000, 3245680000, 3246270000, 3246280000, 3246480000, 3246490000, 3246690000, 3246700000, 3246940000, 3246970000, 3246980000, 3247020000, 3247030000, 3247130000, 3247140000, 3247160000, 3247170000, 3247250000, 3247310000, 3247440000, 3247470000, 3247670000, 3247680000, 324780000, 3247810000, 324782, 3247820000, 324796, 3247960000, 324797, 3247970000, 3247980000, 3248070000, 3248080000, 3248190000, 3248200000, 3248230000, 3248300000 and 25 more |
| Model numbers | CT-H25, CT-H50 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2717-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.