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Medium RiskFDA Device
Medical Devices/Surgical Equipment

Stryker Leibinger GmbH & Co. KG: Scopis ENT Software Recalled for Incorrect Surgical Navigation Feedback

Agency Publication Date: May 23, 2024
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Summary

Stryker Leibinger GmbH & Co. KG has recalled 705 units of its Scopis ENT Software with TGS (Software Version: NOVA 3.6.0 RC16) used in functional endoscopic sinus surgery. This recall was initiated because unreleased software was incorrectly installed on customer systems, causing the visual feedback on the navigation screen to appear in the wrong location compared to the actual physical position of surgical pointers or suction tools. If you have been treated using one of these systems or operate this equipment, you should be aware that surgeons may receive inaccurate guidance during delicate sinus procedures. Consumers and healthcare providers should contact the manufacturer for further instructions regarding a potential update or corrective action.

Risk

The software defect causes a misalignment between the digital markers on the surgical screen and the actual physical location of the instruments inside the patient's sinus cavity. This visual discrepancy could lead a surgeon to navigate incorrectly, potentially causing accidental damage to sensitive surrounding structures during a procedure.

What You Should Do

  1. Verify if your surgical system is running Scopis ENT Software with TGS version NOVA 3.6.0 RC16 and check for Product Code 8000-021-002 with UDI/DI 07613327514179.
  2. Check the serial number of your unit against the affected list, which includes: 10984, 10110, 10164, 10454, 10762, 10387, 10120, 10252, 10414, 10612, 10408, 10673, 11013, 11032, 10566, 10974, 10326, 10442, 10729, 10681, 10552, 10088, 10476, 10307, 10121, 10371, 10262, 10602, 10613, 10381, 10234, 200774, 10135, 10303, 10257, 10639, 10445, 10684, 10740, 10986, 10413, 10079, 10528, 10565, 10482, 10209, 10574, 10606, 10229, 10214, 10797, 10284, 10465, 10295, 10308, 10763, 10434, 11025, 10578, 10473, 10596, 10624, 10591, 11092, 10758, 10097, 10294, 10597, 10769, 10765, 10513, 11088, 10057, 10337, 10464, 10621, 10699, 10509, 10421, 10549, 10003, 10499, 10661, 10668, 10416, 10654, 10571, 10934, 10798, 11022, 10610, 10766, 10471, 10437, 10648, 10410, 10403, 10159, 10192, 10372, 10189, 10193, 10642, 10390, 10771, 10202, 10806, 10237, 10296, 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, 10959, 11000, 10453, 10055, 10335, 10742, 10649, 10983, 10512, 10958, 10268, 10640, 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, 10336, 10760, 10386, 10347, 10286, 10165, 10041, 10456, 10312, 10417, 10500, 10133, 10224, 10031, 10040, 10100, 10784, 10248, 10423, 10215, 10951, 10092, 10185, 10127, 10112, 10790, 10299, 10316, 10435, 10459, 10075, 10479, 10357, 10627, 10732, 10734, 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, 11005, 10177, 10662, 10166, 10197, 10300, 10406, 10181, 10443, 10331, 10364, 10368, 10592, 10062, 10366, 10349, 10353, 11097, 10155, 10218, 10227, 10230, 10315, 10618, 10021, 10787, 11038, 10365, 10637, 10141, 10525, 10341, 10433, 10696, 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, 10692, 10679, 10082, 10573, 10603, 10267, 10541, 10999, 10169, 10628, 10576, 10345, 10738, 10354, 10238, 10077, 10461, 10172, 10243, 10233, 10327, 11023, 11114, 10450, 10398, 10404, 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, 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.
  3. If you are a medical professional, immediately check your system software version. If the unreleased version is found, contact Stryker Leibinger GmbH & Co. KG for instructions on how to receive the correct software update and report any technical issues.
  4. Patients who have recently undergone sinus surgery utilizing Scopis navigation technology should contact their healthcare provider if they have concerns about their procedure.
  5. For further information or assistance regarding this medical device recall, contact the FDA at 1-888-463-6332.

Your Remedy Options

📋Other Action

Correction of unreleased software installation

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: Scopis ENT Software with TGS (Version: NOVA 3.6.0 RC16)
Model / REF:
8000-021-002
UPC Codes:
07613327514179
Lot Numbers:
8000-021-002

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94456
Status: Active
Manufacturer: Stryker Leibinger GmbH & Co. KG
Sold By: Stryker Leibinger GmbH & Co. KG
Manufactured In: Germany
Units Affected: 705 units
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.