FDA Device recall Z-2705-2016
Double Pump RF Patient Cassette
- FDA Device
- Class II
- terminated
- Published 2016-09-07
On 2016-09-07 the FDA classified a Class II recall of Double Pump RF Patient Cassette by Medical Vision Ab, citing sterility of device may be compromised due to sterile package breakage.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2705-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-05-10 |
| Published | 2016-09-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Medical Vision Ab |
| Distribution | AL, CA, CT, GA, IL, IN, KY, MA, MI, MN, NC, NH, NJ, NY, OH, OK, PA, SD, TN, TX, VA, WI |
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
Sterility of device may be compromised due to sterile package breakage.
Identifiers
| code_info | All lot numbers of Double Pump RF Patient Cassettes delivered to the US, Batch numbers: 13I03, 14A01, 14A06, 14A09, 1…All lot numbers of Double Pump RF Patient Cassettes delivered to the US, Batch 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, and 14J03. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2705-2016%22
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