| Class 2 Device Recall Philips Respironics V60 Ventilator |  |
Date Initiated by Firm | November 02, 2020 |
Date Posted | January 22, 2021 |
Recall Status1 |
Open3, Classified |
Recall Number | Z-0905-2021 |
Recall Event ID |
86697 |
510(K)Number | K082660 |
Product Classification |
Ventilator, continuous, minimal ventilatory support, facility use - Product Code MNT
|
Product | Philips Respironics V60 Ventilator Part Number 1053616 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories. |
Code Information |
Model: V60
Part Number: 1053616
V60 Ventilator, English Opt: None
Serial Numbers:
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100087738
100087932
100087999
100088155
100004031
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Amended 07/29/2021: US Products that Faceplates will be replaced
Model: V60
Part Number: 1053616
V60 Ventilator, English Opt: None
Serial Numbers:
100004031
100004071
100004073
100005244
100005350
100005351
100005599
100006209
100006210
100006217
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100011344
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100017293
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100026620
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100033328
100033329
100033330
100033332
100033333
100033334
100033335
100033336
100033338
100033339
100033340
100033342
100033454
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100035744
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100037043
100037044
100037049
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100038936
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100095634
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100097922
100097924
100097926
100097927
100104724
201001172
201001189
201001254
201001255
201001256
201001259
201001260
201001682
201001683
201001696
201001699
201001700
201001720
201001729
201001808
201001812
201001814
201001823
201001825
201001826
201001827
201001829
201001830
201001843
201001849
201001873
201001884
201001939
201001944
201002117
201002148
201002184
201002193
201002426
201002427
201002443
201002445
201002448
201002552
201002566
201002574
201002587
201002770
201002778
201002834
201002868
201002873
201002894
201002899
201002900
201003014
201003145
201003149
201003179
201003183
201003185
201003187
201003216
201003219
201003233
201003238
201003263
201003266
201003268
201003269
201003272
201003273
201006557
|
Recalling Firm/ Manufacturer |
Respironics California, LLC 2271 Cosmos Ct Carlsbad CA 92011-1517
|
For Additional Information Contact | 800-722-9377 |
Manufacturer Reason for Recall | Potential issues with ventilator navigation ring interface and liquid ingress:
1) The navigation ring may become inoperative or operate intermittently;
2) The navigation ring may cause ventilator parameter values to change erratically during setting entries and adjustments. |
FDA Determined Cause 2 | Device Design |
Action | On 11/02/2020, the firm sent an "URGENT-MEDICAL DEVICE CORRECTION" Notification Letter via priority mail informing customer that the V60 Ventilators may experience two potential issues with the navigation ring interface (see table below for additional information).
1. The navigation ring may become inoperative or begin operating intermittently.
2. The navigation ring may not behave as expected, making it difficult for the user to change ventilator settings via the touchscreen.
and if clinicians accept an incorrect setting and leaves the patient on the ventilator without responding to the resulting alarms, the patient could sustain serious injuries.
Customers are instructed:
1. When cleaning V60 ventilators, do not allow cleaning agents to pool on the
ventilator surfaces. This is especially important on the device interface.
2. Check setting changes before and after accepting the changes.
3. If the navigation ring becomes inoperative or operates intermittently during
clinical use, use the touchscreen for all settings changes and navigation,
and contact Philips to schedule service following clinical use.
4. If the navigation ring interferes with your ability to adjust therapy settings via
touchscreen, remove the ventilator from service and contact Philips for
repair.
and to please review the following sections of the user manual:
1. Chapter 10: Care and maintenance. To prevent possible damage to the
ventilator when cleaning, use only those cleaning and disinfecting agents
listed, and do not drip or spray any liquids directly onto any ventilator
surface.
2. Chapter 1: Warnings, cautions, and notes. During clinical use of the
ventilator, monitor patients for changes in respiratory status with each
ventilator setting adjustment. Use an external oxygen monitor to verify
oxygen concentration, and have an alternative means of ventilation available
whenever a ventilator is in use.
Customers are also instructed to complete, sign and return the Acknowledgement and Receipt |
Quantity in Commerce | 330 systems (Amended on 07/29/2021 - 44,841 U.S. systems for faceplate replacement) |
Distribution | Worldwide distribution - US Nationwide including Guam and Puerto Rico; Afghanistan, Albania, Algeria, Andorra, Argentina, Australia, Austria, Bahrain, Bangladesh, Belgium, Bhutan, Bolivia, Brazil, Bulgaria, Burkina Faso, Cambodia, Canada, Chile, China, Colombia, Croatia, Cyprus, Czech Republic, Denmark, Ecuador, Egypt, Ethiopia, Finland, France, French Guiana, French Polynesia, Germany, Ghana, Gibraltar, Greece, Guatemala, Hong Kong, Hungary, Iceland, India, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jersey, Jordan, Kazakhstan, Kenya, Latvia, Lebanon, Libya, Luxembourg, Malaysia, Maldives, Mali, Malta, Mexico, Monaco, Mongolia, Morocco, Myanmar, Namibia, Nepal, Netherlands, New Caledonia, New Zealand, Nigeria, Norway, Oman, Pakistan, Palestine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, Reunion, Romania, Russian Fed., Saudi Arabia, Singapore, Slovenia, South Africa, South Korea, Spain, ST. Pier Miquel, Sweden, Switzerland, Taiwan, Tanzania, Thailand, Turkey, Ukraine, United Arab Emirates, United Kingdom, Venezuela, Vietnam, Wallis Futuna, and Zambia. |
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 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
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510(K) Database | 510(K)s with Product Code = MNT
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