FDA Device recall Z-0569-2015
1488 HD 3-Chip 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 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-0569-2015 |
| 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 Camera; Model Number 1488-210-105 - 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 1488-210-105: 1488 HD 3-Chip Camera head, C-Mount; Serial numbers: 12D020574 12D020584 12D020594 12D020614…Model 1488-210-105: 1488 HD 3-Chip Camera head, C-Mount; Serial numbers: 12D020574 12D020584 12D020594 12D020614 12D020624 12D020634 12D020704 12D020714 12D020734 12E036114 12E036124 12E036134 12E036144 12E036154 12E036164 12E036174 12E036184 12E036204 12E036214 12E036244 12E036254 12E036264 12E036274 12E036284 12E036294 12E036314 12E036324 12E036334 12E036354 12E036374 12E036384 12E036394 12E036404 12E036414 12E036434 12E036444 12E036454 12E038334 12E038344 12E038354 12E038364 12E038374 12E038384 12E038394 12E038404 12E038414 12E038674 12E038684 12E038714 12E038724 12E038754 12E038764 12E039074 12E039084 12E039094 12E039104 12E039114 12E039124 12E039154 12E039164 12E039184 12E039194 12E039204 12E039214 12E039234 12E039244 12E039254 12E039274 12E039284 12E039294 12E039324 12E039334 12E039344 12E039364 12E040514 12E040524 12E040534 12E040544 12E040564 12E040584 12E040594 12E040604 12E040624 12E040634 1 |
|---|
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-0569-2015%22
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