Reported Jan 23, 2013 · Terminated

Microplate, truncated V-bottomed lots included in the above listed products Product Number: 1380 5465. DBS Microplate…

Perkinelmer

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: Perkinelmer · 940 Winter Street · Waltham, MA · 02451

Is this the product you have?

  • Microplate, truncated V-bottomed lots included in the
  • above listed products Product Number1380 5465. DBS Microplate is a general purpose 96 well microplate used in the preparation and examination of specimens from the human body
Lot codes and dates
  • Lot Numbers
    • 616792
    • 617141
    • 617980
    • 618319
    • 618664
    • 618831
    • 619175
Amount recalled
N/A

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

  • Nationwide

Why it was recalled

Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

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.

Free recall alerts

Get alerted about new Perkinelmer recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 7, 2014 · Data as of Sep 19, 4:49 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.