Perkinelmer: Medical Device Recall in 2013 - (Recall #: Z-0689-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

DBS MICROPLATE, TRUNCATED V-BOTTOMED Product Number: 3033-0010

Product Classification:

Class II

Date Initiated: November 26, 2012

Date Posted: January 23, 2013

Recall Number: Z-0689-2013

Event ID: 63771

Reason for Recall:

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

Status: Terminated

Product Quantity: 56 kits (100 plates/kit)

Code Information:

Lot Numbers: 618609

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated