| Class 2 Device Recall BrightView |  |
Date Initiated by Firm | November 30, 2023 |
Date Posted | January 05, 2024 |
Recall Status1 |
Open3, Classified |
Recall Number | Z-0677-2024 |
Recall Event ID |
93643 |
510(K)Number | K062298 |
Product Classification |
System, tomography, computed, emission - Product Code KPS
|
Product | BrightView, Gamma Camera System, Product Code 882480. |
Code Information |
No UDI
Serial numbers
4000002
4000262
4000681
4000218
4000413
4000312
4000389
4000678
4000484
4000288
4000393
4000393
4000494
4000354
4000699
4000515
4000679
4000479
4000689
4000082
4000373
4000471
4000545
4000331
4000038
4000002
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4000164
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4000175
4000244
4000186
4000242
4000235
4000255
4000247
4000320
4000347
4000367
4000402
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4000591
4000537
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4000529
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4000606
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4000449
7135_11
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4000002.75
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4000336
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4000041
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4000167
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4000125
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4000254
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4000404
4000351
4000687
4000380
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4000352
4000357
4000403
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4000349
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4000489
4000484A
4000384
4000443
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4000446
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4000453
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400054
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4000474
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4000496
4000574
4000502
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4000565
4000513
4000433
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4000506
4000476
4000507
4000508
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4000528
4000521
4000523
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4000522
4000534
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4000525
4000541
4000535
4000542
4000556
4000546
4000538
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4000608
4000622
4000623
4000628
4000625
4000629
4000632
4000685
4000630
4000658
4000654
4000635
4000657
4000659
4000649
4000646
4000661
4000650
4000656
4000660
4000653
4000668
4000666
4000684
4000677
4000670
4000671
4000673
4000680
4000695
4000697
4000201
4000527
4000543
5000916 |
Recalling Firm/ Manufacturer |
Philips North America 222 Jacobs St Cambridge MA 02141-2296
|
For Additional Information Contact | Philips Customer Care Solutions Center 800-722-9377 |
Manufacturer Reason for Recall | While using Pre-Programmed Motion during an extrinsic quality assurance scan, a gap is created between the patient support and the detector, which may present a potential extremity entrapment hazard. Risk to patients may include fracture, body part loss of function/debilitation, muscle or ligament sprain or strain, laceration, crush injury, abrasion, or
contusion. |
FDA Determined Cause 2 | Device Design |
Action | On November 30, 2023, the firm notified customers of the issue through Urgent Medical Device Correction Letters.
Users were instructed to monitor the patient during system movement when Pre-Programed Motion is in use and review the warning and caution guidance information provided with the recall notice, and which is also outlined in the Instructions for Use.
Philips will contact you to schedule a time for a field service engineer to visit your site and install a technical solution to resolve this issue.
If you need any further information or support concerning this issue, please contact your local Philips representative: For North America, contact the Customer Care Solutions Center (1-800-722-9377). |
Quantity in Commerce | 359 US; 328 OUS |
Distribution | Domestic distribution nationwide. Foreign distribution worldwide. |
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 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 = KPS
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