FDA Device recall Z-2681-2016
PCR Compano Basic Reader using 100-127V as mains voltage
- FDA Device
- Class II
- terminated
- Published 2016-09-07
On 2016-09-07 the FDA classified a Class II recall of PCR Compano Basic Reader using 100-127V as mains voltage by Philips Electronics North America, citing A defect component of the Compano reader power supply can cause the power supply to burn and some smoke to leave the housing.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2681-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-08-12 |
| Published | 2016-09-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Philips Electronics North America |
| Distribution | AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NM, NV, NY, OH, OR, PA, TX, VT, WA, WI, WV, WY |
Product
PCR Compano Basic Reader using 100-127V as mains voltage. Model numbers: 732027, 732028, and 732040. Radiological image processing system (Computed Radiography).
Reason
A defect component of the Compano reader power supply can cause the power supply to burn and some smoke to leave the housing.
Identifiers
| code_info | Serial Numbers: 2704471 2704473 16620843 16620844 16620845 16720992 16721001 17121932 26523285 26523287 26523…Serial Numbers: 2704471 2704473 16620843 16620844 16620845 16720992 16721001 17121932 26523285 26523287 26523292 26824120 26924172 26924179 27024418 27124646 27124650 27224878 27225020 36125096 36225366 36225367 36225370 36225371 36225372 36225373 36225429 36225431 36225432 36225437 36225438 36325634 36325635 36325639 36325641 36325805 36325810 36325811 36325812 36325813 36325814 36325819 36325820 36425835 36425837 36425838 36425839 36425842 36526123 36526129 36526134 36526135 36526138 36526139 36526140 36526141 36526142 36526144 36526201 36526202 36526206 36526211 36526212 36526213 36626333 36726559 36726560 36726562 36826721 36826722 36826726 36826728 36926990 36926991 37127470 37127472 37127473 46127902 46127903 46127905 46127906 46127909 46127910 46127911 46127912 46127913 46127914 46127992 46127994 46127997 46128000 46128001 46128003 46128004 46128008 46128009 46128010 46128011 462282 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2681-2016%22
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