FDA Device recall Z-1594-2014
SHUNT KIT 9733605 NON-INVASIVE
- FDA Device
- Class II
- terminated
- Published 2014-11-26
On 2014-11-26 the FDA classified a Class II recall of SHUNT KIT 9733605 NON-INVASIVE by Medtronic Navigation, citing medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriat….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1594-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-04-24 |
| Published | 2014-11-26 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Medtronic Navigation |
| Distribution | US |
Product
SHUNT KIT 9733605 NON-INVASIVE
Reason
Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.
Identifiers
| code_info | Lot No.: 120628B 130204E 130314H 121113H 130508B 130612A 130709 130325 130710 130729A 130826 130923B 131016C 131025F 130923B 131127A |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1594-2014%22
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