VOLISTA StandOP (model 600) surgical lights shipped from October 2012 until June 2017 equipped wi...
FDA Device Recall #Z-1937-2018 — Class II — April 19, 2018
Recall Summary
| Recall Number | Z-1937-2018 |
| Classification | Class II — Moderate risk |
| Date Initiated | April 19, 2018 |
| Status | Terminated |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Maquet SAS |
| Location | Orleans, N/A |
| Product Type | Devices |
| Quantity | 187 |
Product Description
VOLISTA StandOP (model 600) surgical lights shipped from October 2012 until June 2017 equipped with keypads with Ref. ARD568801560; Part numbers: 568811901, VLT600SF AIM STP; 568811911, VLT600SF AIM STP; 568811961, VLT600DF AIM STP; 568821910, VLT600SF STP QL; 568821911, VLT600SF AIM STP QL; 568821960, VLT600DF STP QL; 568821961, VLT600DF AIM STP QL VOLISTA surgical lights are intended to be used to provide visible illumination of the surgical area or patient during surgical operations, diagnostics and treatment.
Reason for Recall
Potential keypad failure on VOLISTA StandOP Surgical Lights.
Distribution Pattern
Worldwide Distribution: US (nationwide) and countries of: (AE, AR, AT, AU, BD, BE, BO, BR, CA, CH, CL, CM, CN, CO, CZ, DE, DK, EC, EE, EG, ES, Fl, FR, GB, GH, HK, HR, HU, IE, IN, IQ, IR, IT, JO, JP, KE, KR, LB, LU, LV, MQ, MX, MY, NA, NG, NL, OM, PA, PK, PL, PT, PY, RO, RS, SA, SE, SG, SI, SK, TH, TR, TT, TW, TZ, YE, ZA, ZW).
Lot / Code Information
Serial Numbers: 38013 38016 500641 500644 25002 35025 35028 38012 38015 500000 500001 500003 500004 500014 500015 500016 500018 500037 500039 500020 500060 500063 500642 500643 31053 500058 38009 38026 31002 31030 31048 31054 21001 21002 35024 35012 35013 35014 35015 38017 500001 500017 35029 35017 35027 31019 31020 31022 31024 31025 31026 31000 31000 31001 31002 31003 31006 31009 31010 31012 31008 31047 31050 31051 31052 500002 500060 500061 500072 500073 500680 500685 500686 500687 500692 510082 500062 500064 500042 500044 31012 31013 31014 31020 38011 38014 31006 31008 31015 31016 500068 500070 500071 500074 31021 31023 38018 38019 38020 38021 38022 38023 38024 38025 31004 35011 31004 31017 31018 35000 35001 35018 35019 35020 35021 35022 35023 35026 35030 35031 35032 35033 38027 31001 31003 28003 28004 25005 25006 500055 500059 500011 500013 25007 25004 31039 31040 31041 31042 31043 31044 31045 31046 31055 31056 31005 31009 31011 31017 31019 38025 38026 38027 38028 500065 500066 500067 500069 38000 38002 500002 500005 500010 500012 500056 500059 38001 38003 31031 31049 20502 20503 500075 500076 500609 500610 500611 500612 500613 500614 500615 500616 500617 500618 500619 500620 500066 500067 500068 500069 500070 500071 500072 500073 510007 510008 510009 510010 510011 510012 510013 510014
Other Recalls from Maquet SAS
| Recall # | Classification | Product | Date |
|---|---|---|---|
| Z-2502-2018 | Class II | VOLISTA StandOP Surgical Light, ARD568811961 ... | Jun 14, 2018 |
Frequently Asked Questions
Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.
Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.
Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.
What Should You Do?
Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.