Reported Nov 19, 2025 · Ongoing
DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 712032;
Philips Medical Systems DMC GmbH
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Philips Medical Systems DMC GmbH · Development And Manufacturing Ctr. · Hamburg · N/A
Is this the product you have?
DigitalDiagnost 4 (1) High Performance(2) Flex/Value
- Model Number
(1) 712031(2) 712032
- Lot codes and dates
6 of 6 products
Products covered by this recall Model / number Barcodes Product as published 712031— — 00884838065321UDI-DI: 00884838065321 — Serial Numbers: 10001181, 10001182, 10001185, 10001186, 10001188, 10001189, SN16000022, SN20000013 712032— — 00884838074514UDI-DI: 00884838074514 — Serial Numbers: 10001179, 19000341, 19000342, 19000343 - Amount recalled
- 12 units
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
- Nationwide
Why it was recalled
Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.
This product could cause temporary or reversible health problems — stop using it.
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