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.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot Numbers: 616792 , 617141 , 617980 , 618319, 618664, 618831, 619175
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Perkinelmer
Reason for Recall:
Truncated V-Bottomed Microplate Wells used in assays contain defective wells.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

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.

Product Codes/Lot Numbers:

Lot Numbers: 616792 , 617141 , 617980 , 618319, 618664, 618831, 619175

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0690-2013

Related Recalls

Defective tips have the potential to pipette/dispense volumes 50-100% lower than is specified for the tips.

Oct 13, 2016 Other Medical Devices View Details →

Filter Tips molded incorrectly and may not seal to the Varispan tip adaptor properly causing inaccurate aspiration and dispensing

Jun 24, 2016 Surgical Instruments View Details →

The content of the second #023 barcode ID label in the Barcode ID Label Binder is incorrect. The second barcode ID label #023 symbol incorrectly identifies as #024 when scanned. If measurement protocols have been programmed for both ID #023 and #024, the protocol associated with barcode ID #024 is executed. If the error is undetected, the Gamma Counter may produce erroneous results.

Dec 8, 2015 Other Medical Devices Nationwide View Details →