Reported Nov 15, 2023 · Ongoing
DigitalDiagnost 4 Chest/Emergency, used to acquire, process, store, display and export digital radiographic images.
Philips North America LLC
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 North America Llc · 222 Jacobs St · Cambridge, MA · 02141-2289
Is this the product you have?
- DigitalDiagnost 4 Chest/Emergency, used to acquire, process, store, display and export digital radiographic images.
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Barcodes Product as published 712029& 712033 — 008848380745210088483807452100884838074521008848380745210088483807452100884838074521008848380745210088483807452100884838074521008848380745210088483807452100884838074521UDI: (01)00884838074521(21) SN19000272, (01)00884838074521(21) SN19000213 , (01)00884838074521(21) 10001077, (01)00884838074521(21) SN20000097, (01)00884838074521(21) SN16000074, (01)00884838074521(21) SN15000238, (01)00884838074521(21) SN16000075, (01)00884838074521(21) SN15000367, (01)00884838074521(21) SN18000428, (01)00884838074521(21) SN17000318, (01)00884838074521(21) SN18000309, (01)00884838074521(21) SN18000204 — Serial No. SN15000409, SN19000272, SN19000213, 10001077, SN20000097, SN16000074, SN15000238, SN16000075, SN15000367, SN18000428, SN17000318, SN18000309, SN18000204. - Amount recalled
- 13 units
This recall covers 10 products
The agency filed one notice per product. You are reading one of them; the other 9 are below.
Where it was sold
- Nationwide
Why it was recalled
Potential for units suspended on the ceiling to fail and fall.
This product could cause temporary or reversible health problems — stop using it.
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