Reported Jun 26, 2013 · Terminated
Philips Diagnost Stationary Radiographic System Models: 712020, 712022, 712050, 712052, 712055, 712057, 712062 Product…
Philips Healthcare 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 Healthcare Inc. · 3000 Minuteman Road · Andover, MA · 01810
Is this the product you have?
- Philips Diagnost
- Stationary Radiographic System Models
712020712022712050712052712055712057712062
- Product UsageUniversal RAD Applications
- Lot codes and dates
- Serial Numbers
175 of 175 codes
2482443518963040093477263401843533183162363572753569833259393259406026037020093489973622513561533561313510833563343556483556463542563556443565263624387212356359439357888355621370816357413367356358322363680358494700028136367070346536367136777137595236595637248537248636954570700372973374374375370380750/SN0702498385560/SN0802190401126/SN0802540396834/SN0802370414494/SN0802648429753/SN0902090434680/SN0902161379200/SN0802088390276/SN0802289390109/SN0802396383893/SN0802238
- Serial Numbers
- Amount recalled
- 177 units
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
- Nationwide
Why it was recalled
Installation Acceptance Test Document (IATD) non compliant with regulations IATDs (Installation Acceptance Test could not be located or different templates have been used
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.
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