Class II — the FDA judged the product may cause temporary or medically reversible harm, with a remote chance of serious harm.
This is the FDA's risk judgment for this recall. It describes the potential of the product as a category — it does not establish that any specific unit harmed anyone. Most recalls are Class II or III.
8000-021-002, Scopis¿ ENT Software with TGS¿ with Sofware Version: NOVA 3.6.0 RC16. Scopis is a next-generation solution for navigating functional endoscopic sinus surgery (FESS) offering surgeons highly advanced image guidance and visualization capabilities in a single system. The Stryker Electromagnetic Navigation Unit (8000-010-003) powered by Scopis ENT Software with TGS (8000-021-002), allows the analysis and identification of sinus cells in the complex patient anatomy and planning of the natural drainage pathways through the sinus cavity. During surgery, the planned pathways are overlaid in real-time onto the endoscopic image, providing a unique Scopis augmented reality technology. Guidance of endoscopic instruments may help perform a minimally invasive, accurate and selective surgery.
Why it was recalled
Unreleased software was installed on customer systems resulting in the visual feedback on the screen to show the points to be off from the physical reference point of the pointer or suction.
Is your unit affected?
The recall covers only the specific lots or serial numbers the FDA listed. Enter the lot or serial number from your product's label and we'll check it against that list.
A match means your unit may be covered — stop and call your pharmacist before doing anything. No match suggests it isn't covered, but confirm anyway: code formats vary and lists can be incomplete. Your unit not being listed does not guarantee it is safe, and being listed does not mean you have been harmed.
Show the FDA's listed lot / code information
Sofware Version: NOVA 3.6.0 RC16, Product Code: 8000-021-002; UDI/DI: 07613327514179; Serial Numbers: 10984, 10110, 10164, 10454, 10762, 10387, 10120, 10252, 10414, 10612, 10408, 10673, 11013, 11032, 10566, 10974, 0310-B, 10326, 10442, 10729, 10681, 10552, 10088, 10476, 10307, 10121, 10371, 0252-B, 10262, 10602, 10613, 10381, 10234, 200774, 10135, 0304-B, 10303, 10257, 10639, 10445, 10684, 10740, 10986, 10413, 10079, 10528, 10565, 10482, 10209, 10574, 10606, 10229, 10214, 10797, 0335-B, 10284, 10465, 10295, 10308, 0282-B, 83B750AD, 0287-B, 10763, 10434, 11025, 10578, 10473, 10596, 0291-B, 10624, 10591, 11092, 10758, 10097, 10294, 0251-B, 10597, 10769, 0309-B, 10765, 0313-B, 0281-B, 10513, 11088, 10057, 10337, 10464, 10621, 10699, 10509, 10421, 10549, 10003, 10499, 10661, 10668, 0292-B, 10416, 0263-B, 10654, 10571, 0329-B, 10934, 10798, 11022, 10610, 10766, 10471, 10437, 10648, 10410, 10403, 10159, 10192, 10372, 10189, 10193, 10642, 10390, 10771, 10202, 10806, 10237, 10296, 0244-B, 0307-B, 10034, 10440, 10704, 10101, 10153, 10098, 10388, 10720, 10943, 10944, 10994, 10695, 10608, 10615, 10054, 10076, 10015, 10089, 10208, 10776, 10780, 11111, 10586, 10759, 10431, 10772, 10376, 10563, 10978, 10989, 10369, 10641, 10796, 10558, 10660, 10071, 10987, 10953, 10982, 10744, 10026, 0325-B, 10959, 11000, 10453, 0332-B, 10055, 10335, 10742, 10649, 10983, 10512, 10958, 10268, 10640, 0280-B, 11075, 11117, 10356, 10429, 10432, 10659, 10677, 10319, 10311, 10332, 10757, 10809, 10523, 10382, 10451, 10495, 10997, 11116, 11018, 10083, 10672, 10775, 10053, 10195, 10330, 10161, 10007, 10328, 10949, 11031, 10781, 10990, 10350, 10750, 10191, 10033, 10056, 10446, 10078, 10516, 10373, 10722, 10136, 10210, 10091, 10255, 10253, 10060, 10427, 10162, 10297, 10731, 10935, 0285-B, 10336, 10760, 10386, 10347, 10286, 10165, 10041, 10456, 10312, 10417, 10500, 10133, 10224, 10031, 10040, 10100, 10784, 10248, 10423, 10215, 10951, 10092, 0260-B, 10185, 10127, 10112, 10790, 10299, 10316, 10435, 10459, 10075, 10479, 10357, 10627, 10732, 10734, 0343-B, 0320-B, 10517, 10455, 10590, 11030, 10383, 10043, 10096, 10789, 10631, 10489, 10791, 10220, 10658, 10348, 10143, 10114, 10625, 10799, 11108, 10103, 10522, 10126, 10066, 10980, 11102, 0318-B, 11005, 10177, 10662, 10166, 10197, 10300, 10406, 10181, 0326-B, 10443, 10331, 10364, 10368, 10592, 10062, 10366, 10349, 10353, 11097, 10155, 10218, 10227, 10230, 10315, 10618, 10021, 10787, 11038, 0271-B, 10365, 10637, 10141, 10525, 10341, 10433, 10696, 0333-B, 10401, 10633, 10211, 10231, 10052, 10794, 10685, 10157, 10213, 10081, 10123, 10090, 10199, 10678, 11020, 10216, 10377, 10424, 10212, 10361, 10059, 10109, 10736, 10344, 10693, 10977, 11004, 10016, 10168, 10171, 10691, 10006, 10458, 10324, 10156, 10190, 10221, 10363, 10475, 0322-B, 0339-B, 10692, 10679, 10082, 10573, 10603, 10267, 10541, 10999, 10169, 10628, 10576, 10345, 10738, 10354, 10238, 0259-B, 10077, 0306-B, 10461, 10172, 10243, 10233, 10327, 0327-B, 11023, 11114, 10450, 10398, 10404, 0303-B, 10400, 10412, 10593, 10072, 10514, 10239, 10069, 10244, 10249, 10761, 10359, 10739, 10352, 10163, 10374, 10698, 10342, 10607, 10635, 10058, 10425, 10419, 10950, 10405, 10422, 10223, 0308-B, 10010, 10594, 10205, 10370, 10474, 10247, 10020, 10174, 10184, 10188, 10128, 11003, 10689, 10701, 10795, 10074, 10266, 10288, 10008, 10203, 10966, 10438, 10955, 10073, 10080, 10333, 10777, 10508, 10325, 10086, 10104, 10469, 10755, 10810, 10671, 10152, 10393, 10657, 10105, 10298, 10524, 10805, 10375, 10402, 10094, 10358, 10498, 10501, 10384, 10391, 10993, 10064, 10175, 10397, 10560, 10570, 10630, 10132, 10579, 10439, 10415, 10306, 10343, 10477, 10323, 10737, 10589, 10304, 10338, 10460, 10598, 10779, 10988, 10346, 11082, 10436, 10362, 10334, 10682, 10653, 10583, 10724, 10725, 10407, 10380, 10409, 10595, 10137, 10656, 10389, 10611, 10638, 11036, 11037, 10577, 10609, 10587, 10626, 10965, 11017, 11112, 10547, 10954, 11029, 11026, 10979, 10985, 11080, 10981, 11099, 10207, 10049, 10580, 10144, 10723.
Recall status
Ongoing — the recall is still being carried out.
Where it was distributed
US Nationwide distribution.
Recall record
- Recalling firm
- Stryker Leibinger GmbH & Co. KG
- Product type
- Devices
- Recall number
- Z-1885-2024
- Voluntary / mandated
- Voluntary: Firm initiated
- Initial notification
- Letter
- Origin
- Freiburg Im Breisgau
- Recall initiated
- 2024-04-04
What to do
Check the lot/code above against your product. To confirm this record and read the FDA's full notice, see the FDA recall page. Before changing anything you take or use, ask your pharmacist or prescriber — this page does not tell you to start or stop any drug or device.
Also available: structured data (JSON-LD) · recall record (JSON)
What this is — and is not
A recall is a recorded FDA enforcement action — the FDA logged that a firm is removing or correcting a product. It does not establish that any specific unit harmed anyone, and causation is not established by a recall. The class above is the FDA's risk judgment for the product category, not a finding about your unit. This page informs and compares; it is not medical advice and never tells you to start or stop a drug or device.
To report a problem you experienced, use
FDA MedWatch.
Verify this record at FDA recalls ·
Recall Z-1885-2024 · Source: openFDA enforcement.