Reported Apr 24, 2024 · Ongoing
MR 7700, Magnetic Resonance System.
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?
- MR 7700, Magnetic Resonance System.
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Barcodes Product as published 782120— — 884838104112UDI-DI 884838104112 — Serial No. 65051, 65005, 65000, 65002, 65003, 65001, 65004, 65009, 65012, 65013, 65015, 65017, 65020, 65019, 65021, 65023, 65024, 65025, 65031, 65006, 65032, 65035, 65034, 65038, 65030, 65037. - Amount recalled
- 26 units
This recall covers 41 products
The agency filed one notice per product. You are reading one of them; the other 40 are below.
28 more are in the archive.
Where it was sold
- Nationwide
- GA
Why it was recalled
Patient support table floor plate may be incorrectly installed.
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 North America LLC 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.