Reported Aug 5, 2026 · Ongoing · Updated Sep 16, 2026
GEM Premier 5000 with IQM2 Model/Catalog Number: 00024019255 and GEM Premier 7000 with iQM3 Model/Catalog Number:…
Instrumentation Laboratory
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: Instrumentation Laboratory · 180 Hartwell Rd · Bedford, MA · 01730-2443
Is this the product you have?
- GEM Premier 5000
- with IQM2 Model/Catalog Number00024019255 and GEM Premier 7000
- with iQM3 Model/Catalog Number00000015279 Portable blood analyzer system
- Affected AccessoryBar Code Reader (BCR) Wand Part No. 00024015859
- Lot codes and dates
- GEM Premier 5000 Part number00024019255
- UDI08426950870227
- GEM Premier 7000 Part number00000015279
- UDI0195226000924
- Affected AccessoryBar Code Reader (BCR) Wand that received a configuration update on or after 8 April 2026. Part No. 00024015859; UDI No. 08426950869634
- Amount recalled
- 122
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
- Nationwide
Why it was recalled
Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.
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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