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U.S. Department of Health and Human Services

Class 2 Device Recall Trumpf

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  Class 2 Device Recall Trumpf see related information
Date Initiated by Firm July 27, 2015
Date Posted August 07, 2015
Recall Status1 Terminated 3 on May 03, 2017
Recall Number Z-2353-2015
Recall Event ID 71718
510(K)Number K061317  
Product Classification Light, surgical, ceiling mounted - Product Code FSY
Product Trumpf Ceiling Mounted Surgical Lighting Systems,iLED 3/5, User Manual #1558932.

The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
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.
Recalling Firm/
Manufacturer		 Trumpf Medical Systems, Inc.
1046 Legrand Blvd
Charleston SC 29492-7672
For Additional Information Contact Lindsey Ronnenberg
843-822-6939
Manufacturer Reason
for Recall		 Complaints received of the front joint of the spring arm AC 2000 could break at the interface to the monitor.
FDA Determined
Cause 2		 Process control
Action Consignees were notified by letter on/about 7/27/2015.
Quantity in Commerce 9,287 units (total)
Distribution 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.*
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database 510(K)s with Product Code = FSY and Original Applicant = TRUMPF KREUZER MEDIZIN SYSTEME GMBH + CO.KG
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