FDA Device recall Z-0780-2017
PerkinElmer 20ul Clear RoboRack Tip, Pipette (Qty 960) Item Number: 6000677
- FDA Device
- Class II
- terminated
- Published 2016-12-28
On 2016-12-28 the FDA classified a Class II recall of PerkinElmer 20ul Clear RoboRack Tip, Pipette (Qty 960) Item Number: 6000677 by Perkinelmer, citing defective tips have the potential to pipette/dispense volumes 50-100% lower than is specified for the tips.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0780-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-10-13 |
| Published | 2016-12-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Perkinelmer |
| Distribution | IA, MD, NY, WA |
Product
PerkinElmer 20ul Clear RoboRack Tip, Pipette (Qty 960) Item Number: 6000677. Used with the: JANUS AUTOMATED WORKSTATION Product Codes: AJS4001, AJM4001, AJI4001, AJL4001, AJS8001, AJM8001, AJI8001, AJL8001, AJM4G01, AJI4G01, AJL4G01, AJM8G01, AJI8G01, AJL8G01, AJM4M01, AJI4M01, AJL4M01, AJM8M01, AJI8M01, AJL8M01 NGS EXPRESS Product Codes: AJS4NGS
Reason
Defective tips have the potential to pipette/dispense volumes 50-100% lower than is specified for the tips.
Identifiers
| code_info | Lot Codes: 16091338, 16150558, 16091337, 16150559, 16160100, 16160099 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0780-2017%22
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