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Alcon announced a top-priority recall of the Constellation Vision System because of various malfunctions, the U. Food and Drug Administration announced July The Class 1 recall affects all Constellation models manufactured and distributed between Sept. Reports may be filed online at www.
To send reports via mail, users must download FDA form and send in the completed pre-addressed, postage-paid form. Customers may call their Alcon Surgical sales representative or Alcon Technical Consumer Affairs department at , menu option 8, for assistance or additional information. The FDA recall notice is available here. Alcon initiated the recall on April 30 and sent a letter to all Constellation users on July 2 describing potential malfunctions.
The letter also informed users that Alcon representatives will visit all U. Healio News Ophthalmology Ophthalmic Business. Read next. July 21, Tips, tricks, what to dos and what not to dos on how you can save money as a healthcare provider on your commercial real estate Part 1.
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WebApr 17, аи for Recall. Alcon is conducting a Medical Device Removal for the Constellation Pneumatic Handpiece, DSP, product number This action is being . WebMedtronic Recalls MiniMed Insulin Pumps for Incorrect Dosing. Allergan Breast Implant Recall. Recall of Zimmer Implants. Another Happy Client!. WebMar 19, аи Reflecting its uncompromising commitment to patient safety, Alcon today announced an immediate, voluntary market withdrawal of the CyPass Micro-Stent from .