FDA Device recall Z-1582-2014
DISP 9730951 STRL SPHERE, 5PK INSERT
- FDA Device
- Class II
- terminated
- Published 2014-11-26
On 2014-11-26 the FDA classified a Class II recall of DISP 9730951 STRL SPHERE, 5PK INSERT 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-1582-2014 |
| 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
DISP 9730951 STRL SPHERE, 5PK INSERT
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.: B155300281 |
|---|
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-1582-2014%22
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