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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 68756

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
July 09, 2014
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Philips Ultrasound, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 2

QLAB 10 Core Module PN 453561704771. QLAB Quantification Software is a software application package designed to view and quantify image data acquired on Philips Medical Systems ultrasound products.

Z-2109-2014
Recall number
Z-2109-2014
Initiated
July 09, 2014
Classification
Class II
Status
Terminated
Recalling firm
Philips Ultrasound, Inc.
Quantity
25 units total (2 units in the US and 23 units outside the US)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The QLAB a2DQ and aCMQ features have a defect that may use incorrect measurement values under specific conditions.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The QLAB a2DQ and aCMQ features have a defect that may use incorrect measurement values under specific conditions.

Code information

*****SYSTEM BASED ID OUTSIDE THE US********** 120F-P213FA35-V41E, 279E-Q21384E8-P41D, 3FBF-X2649F25-J4BF, 47FD-Q1FD112B-J3F0, 4A8F-U24EA0B5-R493, 5570-Q20D1AB2-W410, 5D8C-G1FC9BDE-N3EF, 684B-V2122501-R41A, 6DA2-G232AD5C-S45B, 731B-Q1FC2691-V3EE, 808E-P20C3018-I40E, 88AA-T1FBB144-W3ED, A0CB-I24CCB81-M48F, A0ED-H1F5BC5B-P3E1, AB9B-S236CD11-W463, BE98-V1E4C83A-P3BF, C6A3-H1FFD0F9-X3F5, CBE9-M24BE0E7-Y48D, EEFC-Y22FED8E-S455, EF0D-I20465FB-I3FE, F475-U1F966C3-X3E8, and V49C-R203F0AE-I3FE. ***********Two units shipped in US and one unit shipped outside the US to distributors do not have serial numbers. There are licensing agreements with these distributors that allows the distributors to create their own licensing and serial numbers and/or tracking information.

Distribution pattern

Distributed in the states of CA, IA, KY, MD, NY, PA, UT, VA, WA and WI. Also distributed in Australia, Belgium, Canada, India, Italy, Japan, South Korea, Netherlands, New Zealand, Spain, Sweden, and Switzerland.

device · product 2 of 2

QLAB 10.1 Core Module PN 453561728001. QLAB Quantification Software is a software application package designed to view and quantify image data acquired on Philips Medical Systems ultrasound products.

Z-2110-2014
Recall number
Z-2110-2014
Initiated
July 09, 2014
Classification
Class II
Status
Terminated
Recalling firm
Philips Ultrasound, Inc.
Quantity
59 units total (12 units in the US and 47 units outside the US)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The QLAB a2DQ and aCMQ features have a defect that may use incorrect measurement values under specific conditions.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The QLAB a2DQ and aCMQ features have a defect that may use incorrect measurement values under specific conditions.

Code information

****SYSTEM BASED ID IN THE US*********************** 12DD-14B7BC8B-295F, 25EB-143A3021-2864, 3E1D-145FC2CB-28AF, 5914-14544E46-2898, 5936-13FD3F20-27EA, 91B6-1437E5A0-285F, 9C64-1478F656-28E1, A1DD-14426F8B-2874, AC8B-14838041-28F6, C501-13FAF49F-27E5, CCFB-144184F1-2872, and J57B-147C2B71-28E8. *****SYSTEM BASED ID OUTSIDE THE US************************ 189A-13D31774-2796, 1B4E-13CD97D8-278B, 2B31-1486400F-28FC, 2B42-145AB87C-28A5, 2E29-13D2A227-2795, 3099-147B40D7-28E6, 3B7A-1439BAD4-2863, 4BD4-13C1AE06-2773, 4E88-13BC2E6A-2768, 50E7-149054AD-2910, 512B-13E23661-27B4, 539B-148AD511-2905, 564F-14855575-28FA, 5682-1402BEBC-27F5, 5E5A-14A05E34-2930, 5E6B-1474D6A1-28D9, 611F-146F5705-28CE, 66CB-13B63981-275C, 6BCD-14B067BB-2950, 6ED6-13D14240-2792, 73E9-149FE8E7-292F, 76F2-13C0C36C-2771, 7951-1494E9AF-2919, 7C05-148F6A13-290E, 7C16-1463E280-28B7, 7C49-13E14BC7-27B2, 7C5A-13B5C434-275B, 7EA8-14B5720A-295A, 8465-13D0CCF3-2791, 8C5F-14175D45-281E, 8F35-13BACE83-2765, 91E9-13B54EE7-275A, A46F-1493FF15-2917, B74A-1499H964-2921, C4CE-147D8B58-28EA, D798-14AE1D3A-294B, D7A9-148295A7-28F4, DA5D-147D160B-28E9, DFB4-149D9E66-292A, DFC5-147216D3-28D3, E268-14981ECA-291F, E7BF-14B8A725-2960, EA95-145C1863-28A7, ED7C-13D4H20E-2797, F598-13C3833A-2776, FDA3-13DE8BF9-27AC, and XAF4-1445A4A6-287B.

Distribution pattern

Distributed in the states of CA, IA, KY, MD, NY, PA, UT, VA, WA and WI. Also distributed in Australia, Belgium, Canada, India, Italy, Japan, South Korea, Netherlands, New Zealand, Spain, Sweden, and Switzerland.