FDA Device recall Z-0029-2020
Embryology Heated Plate within the RI Witness, Model Numbers 6-70-807, 6-70-807-A, & 6-70-807-B - Product Usage: RI Witness uses Radio Freq…
- FDA Device
- Class III
- terminated
- Published 2019-10-09
On 2019-10-09 the FDA classified a Class III recall of Embryology Heated Plate within the RI Witness, Model Numbers 6-70-807, 6-70-807-A, & 6-70-807-B - Product Usage: RI Witness uses Radio Freq… by Coopersurgical, citing the touchpad may not work properly after cleaning.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0029-2020 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2019-09-05 |
| Published | 2019-10-09 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Coopersurgical |
| Distribution | US |
Product
Embryology Heated Plate within the RI Witness, Model Numbers 6-70-807, 6-70-807-A, & 6-70-807-B - Product Usage: RI Witness uses Radio Frequency Identification (RFID) to detect and monitor all activity in the IVF laboratory. The system helps mitigate the risk of human error every time samples are moved from one dish or tube to another, and safeguards every step of the IVF cycle. While the heated plates comprise a heated composite surface with window for a light source. The heated plates comprise a heated composite surface with window for a light source and either sit on top of existing bench-tops or can be integrated to be flush fitted within workstations. Intended use: Provide a favorable temperature environment for the embryo during the IVF procedure.
Reason
The touchpad may not work properly after cleaning.
Identifiers
| code_info | Serial Numbers: 0006 0051 0097 0146 0192 0244 0292 0354 0420 0487 0617 0672 0732 0783 0007 0052 0098 0147 0193 0245 02…Serial Numbers: 0006 0051 0097 0146 0192 0244 0292 0354 0420 0487 0617 0672 0732 0783 0007 0052 0098 0147 0193 0245 0293 0356 0421 0489 0618 0673 0733 0784 0008 0053 0100 0148 0194 0246 0294 0357 0424 0490 0619 0674 0734 0785 0009 0054 0101 0149 0195 0247 0297 0358 0426 0491 0622 0675 0735 0786 0010 0055 0102 0150 0196 0248 0298 0359 0428 0492 0628 0676 0736 0787 0011 0056 0103 0151 0197 0249 0299 0360 0429 0493 0630 0677 0738 0788 0012 0057 0104 0152 0198 0250 0300 0361 0430 0494 0631 0678 0739 0789 0013 0058 0105 0153 0199 0251 0302 0362 0431 0495 0632 0679 0740 0790 0014 0060 0106 0154 0200 0252 0303 0364 0432 0496 0633 0680 0741 0791 0015 0061 0107 0155 0201 0253 0304 0366 0433 0497 0634 0681 0742 0792 0016 0062 0108 0156 0203 0254 0306 0367 0434 0498 0635 0682 0743 0793 0017 0063 0109 0157 0204 0255 0307 0368 0435 0499 0636 0683 0744 0794 0018 0064 0110 0158 0205 0256 0308 0369 0438 0501 0637 0684 0745 0795 0019 0065 0111 0159 0206 0257 0309 0370 0440 0502 0638 0685 0 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0029-2020%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.