Reported Jul 4, 2018 · Terminated
Philips Ingenuity Core 728321
Philips Medical Systems (Cleveland) Inc.
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 (Cleveland) Inc · 595 Miner Rd · Cleveland, OH · 44143-2131
Is this the product you have?
- Philips Ingenuity Core 728321
- Lot codes and dates
5 of 5 products
Products covered by this recall # Barcodes Product as published 1 00884838059498(01)00884838059498(21)333169, Serial Number: 333169 2 00884838059498UDI: (01)00884838059498(21)310377, Serial Number: 310377 3 00884838059498UDI: (01)00884838059498(21)310375, Serial Number: 310375 4 00884838059498UDI: (01)00884838059498(21)333171, Serial Number: 333171 5 00884838059498UDI: (01)00884838059498(21)333172, Serial Number: 333172 - Amount recalled
- 28 total
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
A problem has been detected in the X-Ray Tube. The affected tubes have a production defect that allows oil leakage from the tube housing, if it were to re-occur, could pose a risk for patients or users.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Philips Medical Systems (Cleveland) Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.