FDA Device recall Z-0571-2015
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-0571-2015 |
| 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 1488-610-122 - HD 3-Chip Camera Head with Integrated Coupler. 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 1488-610-122: 1488 HD 3-Chip Camera Head with Integrated Coupler. Serial numbers: 12D030204 12D030214 12D030…Model 1488-610-122: 1488 HD 3-Chip Camera Head with Integrated Coupler. Serial numbers: 12D030204 12D030214 12D030224 12F060834 12F060844 12F060854 12F060874 12F060894 12F060904 12F060914 12F060924 12F060934 12F060954 12F060964 12F060974 12F060984 12F060994 12F061024 12F061054 12F061064 12F061074 12F061084 12F061094 12F061104 12F061114 12F061134 12F061154 12F061164 12F061174 12F061184 12F061194 12F061234 12F061264 12F061274 12F061294 12F061304 12F061314 12F061324 12H001234 12H001244 12H001254 12H001264 12H001274 12H001284 12H001294 12H001304 12H001324 12H038814 12H038824 12H038834 12H038844 12H038854 12H038864 12H038874 12H038894 12H059034 12H059044 12H059054 12H059084 12H059094 12H059104 12H059124 12I004814 12I004834 12I004844 12I004854 12I004864 12I004874 12I004884 12I004894 12I004904 12I004914 12I004954 12I004994 12I005004 12I005014 12I005024 12I005044 12I005054 12I005064 12I005074 12I005084 12I0050 |
|---|
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-0571-2015%22
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