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Trumpf Ceiling Mounted Surgical Lighting Systems,Helion/Xenion S/M/L, User Manual #1441784. Th...

FDA Device Recall #Z-2355-2015 — Class II — July 27, 2015

Recall Summary

Recall Number Z-2355-2015
Classification Class II — Moderate risk
Date Initiated July 27, 2015
Status Terminated
Voluntary Voluntary: Firm initiated

Recalling Firm

Firm Trumpf Medical Systems, Inc.
Location Charleston, SC
Product Type Devices
Quantity 9,287 units total

Product Description

Trumpf Ceiling Mounted Surgical Lighting Systems,Helion/Xenion S/M/L, User Manual #1441784. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.

Reason for Recall

Complaints received of the front joint of the spring arm AC 2000 could break at the interface to the monitor.

Distribution Pattern

Worldwide Distribution-US (nationwide) including Puerto Rico, and the countries of Angola, Antilles, Argentina, Austria, Australia, Azerbaijan, Bosnia and Herzegovina, Belgium, Bulgaria, Bahrain, Brasilia, Belarus, Canada, Switzerland, Chile, China, Columbia, Cyprus, Czech Republic, Germany, Denmark, Algerian, Ecuador, Estonia, Egypt, Spain, Finland, France, Gabon, United Kingdom, Georgian Republic, Greece, Hong Kong, Croatia, Hungary, Indonesia, Ireland, Israel, India, Iraq, Iran, Iceland, Italy, Jordan, Japan, Kenya, South Korea, Kuwait, Kazakhstan, Lebanon, Liechtenstein, Lithuania, Luxembourg, Latvia, Libya, Morocco, Macedonia, Myanmar/Burma, Malta, Mauritius, Mexico, Malaysia, Netherlands, Norway, New Zealand, Peru, Philippines, Pakistan, Poland, Palestine, Portugal, Qatar, Romania, Russia, Saudi Arabia, Sudan, Sweden, Singapore, Slovenia, Slovakia, San Marino, Syria, Thailand, Turkmenistan, Tunisia, Turkey, Taiwan, Ukraine, United Arabian Emirates, Uruguay, Venezuela, British Virgin Islands, Vietnam, Kosovo, Serbia and South Africa.*

Lot / Code Information

The following Material numbers may appear on any of the attached recalled/corrected units: Material #0376288, Description: Federarm 3kg, 3 polig (Swing); 0376289, Federarm 12-18kg, 5-polig Kamera eco; 0376290, Federarm TFT Stop AC 2000, 9-15kg; 0376291, Federarm TFT Stop AC 3000, 12-18kg; 0376292, Federarm TFT Stop Space bis 30kg; 0376293, Federarm 3-polig NRH; 0376294, Federarm 5-polig NRH; 0376295, Federarm 3-polig NRH gerader Abgang; 0376296, Federarm 5-polig NRH gerader Abgang; 0379528, FA AC3000, Stop 7-11KG; 0385719, FA AC 2000 NRH mobil 3p, 12-18kg NG; 1387323, Federarmsicherungssegment AC3000; 1387324, Federarmsicherungssegment AC2000; 1388338, Federarm 12-18 kg 3 polig, HEL2; 1388339, Federarm 12-18 kg 5 polig HEL2; 1388340, Federarm 12-18 kg 9 polig (HELION); 1408906, FA AC2 Stop max 11kg; 1471010, FA AC2000 3p, 12-18kg; 1471011, FA AC2000 Stop 12-18kg; 1471012, FA AC2000 NRH 3p, 12-18kg; 1471013, FA AC2000, 7p, 12-18kg; 1471014, FA AC2000 NRH 7p, 12-18kg; 1471015, FA AC3000 3p, 23-30kg; 1471016, FA AC2000 Stop 6-11kg; 1471017, FA AC2000 TruVidia 7p, 3,5-7kg; 1471018, FA AC2000 Stop 3,5-7kg; 1471351, FA AC3000 NRH 3p, 23-30kg; 1502084, FA AC2 NRH f¿r HEL2, 3POL.; 1504731, Federarm 9-POLIG NRH HEL2; 1507085, (R)FEDERARM AC2000; 1645860, FA AC 2000 NRH mobil 7p, 12-18kg NG; 1645861, FA AC 2000 NRH 7p, 12-18kg NG; 1649687, FA AC 2000 SlimLine STOP, 12-18kg; 1649872, FA AC 2000 SlimLine 3p, 12-18kg; 1649997, Deckenrohr 2f Slimline 1000; 1774143, Ausleger AC2000, 750mm, 3p; 1982310, FA AC2000 MAVIG Protegra2 6-11kg; 1982311, FA AC2000 MAVIG Protegra2 12-18kg; 1982312, FA AC2000 3p, 13,5-21kg; 1982313, FA AC2000 NRH 3p, 13,5-21kg; 4024211, Federarm AC2000; 4024212, FA AC2 Stop; 4024213, FA AC3; 4024214, FA AC3000 Stop, 12-18kg; 4024215, FA AC5000 Stop; 4024651, FA AC3000, 7p; 4024652, FA AC2 3K; 024848, Federarm AC3000 NRH; 4025574, FA AC3000 Stop 23-30 kg; 4025575, FA AC5000 Stop max 15 kg; 4025576, FA AC2 K TruVidia; 8800900, Federarm HELION L+ 12,5 kg 5-polig; 8800901, Federarm HELION M+ 12,5 kg 3-polig; 8800905, Federarm HEL L/L+, 11,4 kg 3-polig; 8800906, Federarm HELION M NRH; 8800907, Federarm FA 77 V 11,4 kg 3 polig; 8800908, Federarm FA 77 V 6,8 kg 3 polig; 8800909, Federarm f¿r L-Leuchte So-Version; 8800910, Federarm f¿r M-Leuchte So-Version; 8800911, Federarm FA 77 V 13 kg 3 polig; 8800915, Federarm FA 77 N 11,4 kg5 polig; 8800916, Federarm FA 77 N 6,8 kg 5 polig; 8800919, Federarm FA 77 N 13 kg 5 polig; 8800920, Federarm FA 77 N 8,9 kg 5 polig; 8800925, Federarm FA 77 N 11,4 kg 7 polig; 8800926, Federarm Helion M NRH 7-polig; 8800929, Federarm FA 77 N 13 kg 7 polig; 8800930, Federarm FA 77 N 8,9 kg 7 polig; 8801000, Federarm HELION M+ 8.3 kg 5-polig; 8801001, Federarm HELION M+ 8,3 kg 3-polig; 8801007, Federarm AC 2000, 9-15 kg O. Elektrik; 8801008, Federarm AC 2000, 7-12 kg 5 polig; 8801009, Federarm AC 2000, 12-18 kg 5 polig; 8801010, Federarm Acrobat 2000 12-18 kg; 8801011, Federarm; 8801012, Federarm AC 2000 7-15 kg 3 polig mit; 8801013, Federarm AC 2000, 9-15 kg 7 polig; 8801014, Federarm f¿r Helion M; 8801015, Federarm AC 2000, 1-3,5 kg 7 polig; 8801016, Federarm AC2000 9-15 kg 5-polig; 8801017, Federarm HELION S Mobile; 8801018, Federarm AC 2000, 12-18 kg 3 polig; 8801019, Federarm AC 2000, 1-3,5 kg 3 polig; 8801020, Federarm AC 2000, 12-18 kg 7 polig; 8801021, Federarm AC 2000, 1-3,5KG, Adapt. Anschl; 8801033, Federarm Deckenanschlu¿ HELS; 8801050, Federarm AC 3000, 12-18 kg ohne Elektr.; 8801051, Federarm SPACE 20-40 kg ohne Elektrik; 8801101, Federarm SWING 2-3 kg 3 POL. 120 Volt; 8801102, Federarm SWING 2-3 kg 3 POL. 230 Volt; 8801103, Federarm f¿r HELION S; 8801104, Federarm SWING 2-3 kg 3 polig; 8807200, Federarm 6.5kg f¿r HELION M+ Mobile; 8894025, Federarm WA 77, 8,3 kg 3 polig; 1425487, FA AC2 STOP 3,5KG - MAX 7KG; 1768718; FA AC 77, NRH 3P; 0385246, FA AC2000 NRH 3P, 12-18KG; 4024790, FA AC3000 NRH 7P; 1419354, FA AC3000 STOP (17 -26KG); 0384021, FA AC2000 NRH MOBIL 3P 12-18KG; 0385247, FA AC2000 NRH MOBIL 7P, 12-18KG; 1695239, ACHSE 1F WL 800, 3P + FA SWING; 1695224, ACHSE 1F ZA 800, 3P + FA SWING; 1886331, BEFESTIGUNGSSET FA AC 77/2000/SWING; and Material #1695225, Description: STATIV MOBIL TL1000, 3P + FA SWING.

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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.

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