Kimberly-Clark RadiOpaque Radiofrequency Cannula — Class II medical device recall Z-0850-2014
Terminated recall by Kimberly-Clark Corporation, reported 2014-02-05, distributed in AZ, CA, DE, FL, LA, MA, MD, NJ…. Product may contain a cannula with an active tip length of only 5mm rather than 10mm as indicated on the label
| Recall number | Z-0850-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Kimberly-Clark Corporation, Roswell, GA, United States |
| Recall initiated | 2013-10-29 |
| Classified | 2014-01-28 |
| Reported by FDA | 2014-02-05 |
| Terminated | 2014-09-03 |
| Distributed | AZ, CA, DE, FL, LA, MA, MD, NJ, NY, OH, PA, TX |
| Reason classes | labeling |
| Lot numbers | M2327K301, M3085K301 |
Product
Kimberly-Clark RadiOpaque Radiofrequency Cannula, Gauge 22, Length 100 mm, Active Tip 10 mm, Distributed in the US by Kimberly-Clark,Product code PMF22-100-10 The product is used to create lesions in nervous tissue when used with the Kimberly-Clark radiofrequency generator and probes.
Reason for recall
Product may contain a cannula with an active tip length of only 5mm rather than 10mm as indicated on the label.
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-0850-2014. 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.