| Class 2 Device Recall JUPITER | |
Date Initiated by Firm | December 03, 2014 |
Date Posted | January 06, 2015 |
Recall Status1 |
Terminated 3 on August 23, 2016 |
Recall Number | Z-0923-2015 |
Recall Event ID |
69927 |
Product Classification |
Table, surgical with orthopedic accessories, ac-powered - Product Code JEA
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Product | IIR remote control JUPITER, Material no.4544120, Serial number: to (incl.) 102006720.
Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer system to the operating theatre or from the operating theatre to the patient transfer system. |
Code Information |
The operating tables which are operated with the affected remote controls (all serial numbers): Mobile column JUPITER System U, Material no. 4500113; Mobile column JUPITER System Miyabi U, Material no. 1574977; Operating table column JUPITER SM 360 U, Material no. 1389824; Operating table column JUPITER SF U OCE, Material no. 1622774; Stationary column JUPITER System U, Material no. 4500112; FLOOR MOUNTING COLUMN JUPITER U, Material no. 1276277; Floor mounting column JUPITER 360 U, Material no.1389826; Operating table JUPITER UNIVERSAL U, Material no. 4500170; OR-TABLE JUPITER UNIVERSAL CARBON U, Material no.1223188. |
Recalling Firm/ Manufacturer |
Trumpf Medical Systems, Inc. 1046 Legrand Blvd Charleston SC 29492-7672
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For Additional Information Contact | Lindsey Ronnenberg 843-534-0606 |
Manufacturer Reason for Recall | Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes |
FDA Determined Cause 2 | Component change control |
Action | Trumpf sent an Urgent Medical Device Correction letter on December 3, 2014, to all affected customers. Customers were instructed to complete and return the Confirmation of Receipt form with serial numbers of the affected table(s) and the serial number(s) for any remote controls they have. Replacement remotes will be sent. Customers were instructed to dispose of their recalled remotes. Customers with questions were instructed to call 888-474-9359.
For questions regarding this recall call 843-534-0606. |
Quantity in Commerce | 3303 total all devices |
Distribution | Worldwide Distribution - USA including AL, AZ, CA, CT, FL, GA, IL, KS, LA, MD, MI, MK, MS, NC, NH, NJ, NY, OH, OK, PA, RI, SC, TX, VA, WA, WI and Internationally to Canada. |
Total Product Life Cycle | TPLC Device Report |
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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.
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