FDA Device recall Z-0690-2013
Microplate, truncated V-bottomed lots included in the above listed products Product Number: 1380 5465
- FDA Device
- Class II
- terminated
- Published 2013-01-23
On 2013-01-23 the FDA classified a Class II recall of Microplate, truncated V-bottomed lots included in the above listed products Product Number: 1380 5465 by Perkinelmer, citing truncated V-Bottomed Microplate Wells used in assays contain defective wells.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0690-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-11-26 |
| Published | 2013-01-23 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Perkinelmer |
| Distribution | US |
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.
Reason
Truncated V-Bottomed Microplate Wells used in assays contain defective wells.
Identifiers
| code_info | Lot Numbers: 616792 , 617141 , 617980 , 618319, 618664, 618831, 619175 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0690-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.