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EnVeo R Loading System, Model No. LS-EnVeoR-23… recallZ-2264-2015 · Medtronic Cardiovascular Surgery-the Heart Valve Division · initiated Jul 15, 2015

Class I Terminated All recalls posted in August 2015

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from Medtronic Cardiovascular Surgery-the Heart Valve Division or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

Medtronic is recalling the EnVeo R Loading Systems because of the presence of particulate.

FDA root cause category: Process control

What the company is doing

An Urgent Medical Device Recall Letter dated July 2015 will be be sent to customers who purchased the EnVeo R Loading System because Medtronic has received 8 reports related to this issue out of 7347 potentially affected units. The letter informs customers of the problems identified and the actions to be taken. Customers are instructed to complete the customer confirmation certificate and to email [email protected] or fax to Medtronic at (651) 367-0612 to the attention of Customer Focused Quality.

Recall details

Recall number
Z-2264-2015
Recall class
Class I (most serious)
Status
Terminated
Initiated by the company
Jul 15, 2015
Posted by the FDA
Aug 5, 2015
Recalling firm
Medtronic Cardiovascular Surgery-the Heart Valve Division
Quantity
6,912 units total (540 units in US)
Product code
NPT
FDA submissions
P130021
Distribution
Worldwide Distribution - US Nationwide, Australia, Austria, Belgium, Canada, Czech Republic, Denmark, Dominican Republic, Estonia, Finland, France, Germany, Greece, Hong Kong, Ireland, Israel, Italy, Kuwait, Latvia, Lithuania, Netherlands, New Zealand, Norway, Philippines, Poland, Portugal, Qatar, Saudi Arabia, Singapore, Slovenia, Spain, Sweden, Switzerland, Turkey, United Arab Emirates and United Kingdom.

Product description

EnVeo R Loading System, Model No. LS-EnVeoR-23, LS-EnVeoR-2629, LS-EnVeoR-23-C, LS-EnVeoR-2629-C. Cardiovascular valve delivery system for use with the Medtronic CoreValve Evolut R system.

Code information (models, lots, serial numbers)

Show the full code information (1k characters)

0007254814 0007266413 0007332504 0007332506 0007332508 0007332510 0007343321 0007343324 0007343327 0007350825 0007350837 0007354113 0007354245 0007366949 0007369883 0007393098 0007393101 0007408862 0007408865 0007408867 0007408869 0007428258 0007428260 0007428263 0007435169 0007439358 0007439360 0007439362 0007456292 0007456298 0007462901 0007462903 0007462905 0007476215 0007476217 0007476219 0007482219 0007482222 0007482226 0007486826 0007492356 0007495691 0007495694 0007495696 0007508883 0007508885 0007508891 0007515698 0007515700 0007515703 0007522595 0007522598 0007522600 0007522603 0007530963 0007530973 0007537892 0007537894 0007569474 0007569477 0007569482 0007573778 0007573785 0007573788 0007573791 0007579940 0007579944 0007579948 0007579951 0007592664 0007592666 0007592669 0007592672 0007598984

Other devices under the same FDA submission

52 devices cleared under P130021 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.

Sources and updates

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