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Perkinelmer recalls Microplate, truncated V-bottomed lots included in the above listed products Product Number: 1380 5465. DBS
Recalled January 23, 2013 · FDA recall Z-0690-2013 · Perkinelmer
Hazard
Truncated V-Bottomed Microplate Wells used in assays contain defective wells. · FDA Class II
Units
N/A
Sold at
Nationwide Distribution.
Description
Truncated V-Bottomed Microplate Wells used in assays contain defective wells.
Product
Microplate, truncated V-bottomed lots included in the above listed products Product Number: 1380 5465. DBS Microplate is a general purpose 96 well microplate used in the preparation and examination of specimens from the human body.
Manufacturer(s)
Perkinelmer
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →