Reported Mar 11, 2020 · Ongoing
Atellica CH Reaction Ring Segment, SMN 11099326, UDI 00630414596143
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. · 511 Benedict Ave · Tarrytown, NY · 10591-5005
Is this the product you have?
Atellica CH Reaction Ring SegmentSMN 11099326UDI 00630414596143
- Lot codes and dates
- Lots***new lots added 3/2/2020***
N1521417N1522218N1528917N1526418N1502518N1527518N1503218N1529618N1503918N1530318N1504618N1531018N1516318N1531618N1517218N1532318N1518318N1535518N1519418N1536318N1520118
N1500119N1520519N1500219N1521319N1500620N1522419N1501119N1523319N1501520N1526719N1503519N1527619N1505619N1528719N1506419N1529619N1507919N1533819N1508519N1534719N1510619N1535719N1519019N1530419N1519719
- Lots
- Amount recalled
- 3559
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
Some lots ending in "17", "18", "19", or higher may have cuvette defects allowing water from the water bath to contaminate the interior of the cuvette, which may falsely elevate or depress sample results.
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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