medical Class II Updated 2018-08-29

Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost, Dual-Detector (Stitching Patient Support) 7

Recalled Product

DigitalDiagnost, Dual-Detector (Stitching Patient Support) 712052


Hazard / Issue

The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Serial Numbers: 363679 404164/SN0802462 378830/SN0802004 341693 358494 359442 396571/SN0802311 359449 346075 382021/SN0802313 374374 404298/SN0802474 402570/SN0802420 373501 373500 382272/SN0802113 368428 382012/SN0702520 376667 356957 392502/SN0802179 407423/SN0802638 359767 368619 358641 357697 381998/SN0702488 413829/SN0802631 358320 400364/SN0802522 404166/SN0802441 356981 390272/SN0802364 390273/SN0802366 412482/SN0802683 348997 396576/SN0802233 372848 373508 383084/SN0802127
View official government recall

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