Reported Nov 13, 2019 · Terminated

VITROS chemistry Products Cl- Slides, Catalog No. 6844471 (which supports Urine CL-). MicroSlides which contain…

Ortho-Clinical Diagnostics

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: Ortho-Clinical Diagnostics · 513 Technology Blvd · Rochester, NY · 14626-3601

Is this the product you have?

  • VITROS chemistry Products Cl- Slides, Catalog No. 6844471 (which supports Urine CL-). MicroSlides which contain reagents in a dry, multi-layered form.
Lot codes and dates
  • 199 of 199 codes

    • 401006613389
    • 401006613500
    • 401006613501
    • 401006613608
    • 401006613609
    • 401006613648
    • 401006613671
    • 401006613712
    • 401006613796
    • 401006613843
    • 401006613890
    • 401006584017
    • 401006614028
    • 401006584103
    • 401006584161
    • 401006584214
    • 401006584259
    • 401006584230
    • 401006644380
    • 401006644436
    • 401006644502
    • 401006644529
    • 401006644574
    • 401006584374
    • 401006644604
    • 401006644649
    • 401006644670
    • 401006644705
    • 401006644745
    • 401006644800
    • 401006644871
    • 401006644893
    • 401006644896
    • 401006664973
    • 401006665040
    • 401006665041
    • 401006665223
    • 401006665225
    • 401006665226
    • 401006665248
    • 401006665295
    • 401006665227
    • 401006665228
    • 401006665229
    • 401006665306
    • 401006675376
    • 401006675473
    • 401006675474
    • 401006675513
    • 401006675514
    • 401006675559
    • 401006675477
    • 401006675478
    • 401006675501
    • 401006675552
    • 401006675553
    • 401006675630
    • 401006675631
    • 401006675659
    • 401006675660
Amount recalled
1365545 total

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

Users may experience intermittent slide dispense issues with some cartridges due to the anti-backup platen failing to advance inside the cartridge.

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Nov 13, 2020 · Data as of Sep 19, 4:50 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.