Reported Jan 13, 2016 · Terminated
Siemens Acute Care CKMB DilPak- an in vitro diagnostic product intended to be used in conjunction with the Acute Care…
Siemens Healthcare Diagnostics 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: Siemens Healthcare Diagnostics Inc · 2 Edgewater Dr · Norwood, MA · 02062-4637
Is this the product you have?
- Siemens Acute Care CKMB DilPak- an in vitro diagnostic product intended to be used in conjunction with the
- Acute Care CKMB TestPak Catalog NumberCCKMB-D
- SMN10445070
- Lot codes and dates
- Lot Numbers845173002
- Amount recalled
- 146
This recall covers 11 products
The agency filed one notice per product. You are reading one of them; the other 10 are below.
Where it was sold
- Nationwide
Why it was recalled
Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
This product could cause temporary or reversible health problems — stop using it.
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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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