Double Pump RF Patient Cassette — Class II medical device recall Z-2705-2016
Terminated recall by Medical Vision Ab, reported 2016-09-07, distributed in AL, CA, CT, GA, IL, IN, KY, MA…. Sterility of device may be compromised due to sterile package breakage.
| Recall number | Z-2705-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medical Vision Ab, Nacka, N/A, Sweden |
| Recall initiated | 2016-05-10 |
| Classified | 2016-08-30 |
| Reported by FDA | 2016-09-07 |
| Terminated | 2017-09-18 |
| Distributed | AL, CA, CT, GA, IL, IN, KY, MA, MI, MN, NC, NH, NJ, NY, OH, OK, PA, SD, TN, TX, VA, WI |
| Quantity | 3,295 devices |
| Reason classes | sterility, device malfunction |
| Lot numbers | 13I03, 14A01, 14A06, 14A09, 14A10, 14B03, 14B09, 14C06, 14C10, 14D07, 14D11, 14E06, 14E10, 14F01, 14F02, 14F03, 14F04, 14F10, 14F11, 14G07, 14H02, 14H04, 14H08, 14H09, 14J01, 14J02, 14J03 |
Product
Double Pump RF Patient Cassette; Product Number: 72204055. Intended to provide fluid distension and irrigation and fluid suction during diagnostic and operative arthroscopic procedures.
Reason for recall
Sterility of device may be compromised due to sterile package breakage.
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-2705-2016. 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.