FDA Device recall Z-0570-2015
1488 HD 3-Chip Inline Camera
- FDA Device
- Class II
- terminated
- Published 2014-12-17
On 2014-12-17 the FDA classified a Class II recall of 1488 HD 3-Chip Inline Camera by Stryker Endoscopy, citing in certain operating room environments, a colored screen image occurs with the 1488 Cameras that were manufactured during a specific time period.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0570-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-03-05 |
| Published | 2014-12-17 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Stryker Endoscopy |
| Distribution | US |
Product
1488 HD 3-Chip Inline Camera; Model Number 1488-710-105 - HD 3-Chip Inline Camera, C-Mount; Product Usage: High definition camera to view endoscopic surgical sites on video monitors and capture still and video images of endoscopic surgical applications. Indicated for use in general laparoscopy, nasopharyngoscopy, ear endoscopy, sinuscopy and plastic surgery wherever a laparoscope/endoscope/arthroscope is indicated for use.
Reason
In certain operating room environments, a colored screen image occurs with the 1488 Cameras that were manufactured during a specific time period
Identifiers
| code_info | Model 1488-710-105: 1488 HD 3-Chip Camera head, C-Mount; Serial numbers: 12F016274 12F016294 12F055824 12F055844…Model 1488-710-105: 1488 HD 3-Chip Camera head, C-Mount; Serial numbers: 12F016274 12F016294 12F055824 12F055844 12F055874 12F055884 12F055894 12F055904 12F055914 12F055924 12F055934 12F055954 12F055964 12F055974 12F055994 12F056004 12F056024 12F056034 12F056054 12F056064 12F056094 12F056104 12F056124 12F056154 12F056164 12F056174 12F056184 12F056194 12F056204 12F056664 12F056674 12F056684 12F056694 12F056704 12F056714 12F056744 12F058884 12F058894 12F058904 12F058924 12F058934 12F058944 12F058964 12G054154 12G054174 12G054194 12G054214 12G054224 12G054234 12G054244 12G054264 12H011414 12H011434 12H011444 12H011454 12H011474 12H011494 12H050834 12H050844 12H050854 12I039444 12I039454 12I039464 12I039474 12I039494 12I039504 12I039524 12I039534 12I040844 12I040854 12I040864 12I040874 12I040894 12I040924 12I040934 12I047324. 12D030204 12D030214 12D030224 12F060834 12F060844 12F060854 12F060874 12F06089 |
|---|
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-0570-2015%22
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