FDA Device recall Z-0525-2021
CME America T-Syringe Pump -T34L - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precis…
- FDA Device
- Class II
- terminated
- Published 2020-12-09
On 2020-12-09 the FDA classified a Class II recall of CME America T-Syringe Pump -T34L - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precis… by Cme America, citing multiple reasons: 1) Due to wear and tear of pump motor block mechanism - may cause under infusion situations without the pump alarm being generated. 2) Due to cracks, pump hardwa….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0525-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-07-30 |
| Published | 2020-12-09 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Cme America |
| Distribution | US |
Product
CME America T-Syringe Pump -T34L - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous, subcutaneous, percutaneous, intra-arterial, epidural, in close proximity to nerves, and into an intra-operative site (soft tissue/body cavity/surgical wound site).
Reason
Multiple reasons: 1) Due to wear and tear of pump motor block mechanism - may cause under infusion situations without the pump alarm being generated. 2) Due to cracks, pump hardware may be damaged by fluid used during the cleaning process.
Identifiers
| code_info | Model TR34L - Part Number(s) 100-100PSLA; 100-101PSLA Serial Number: 58766 58765 26479 69547 69548 26428 26299…Model TR34L - Part Number(s) 100-100PSLA; 100-101PSLA Serial Number: 58766 58765 26479 69547 69548 26428 26299 26301 26295 26294 26304 26296 26298 26302 26297 26300 26130 26133 26132 58906 58907 58909 58910 58911 58912 58913 58914 58915 58916 58917 58918 58919 58920 58921 58922 58923 58924 58925 58926 58998 59003 59007 58999 59006 59000 59004 59002 59005 59001 69618 69619 69628 69629 69630 69637 69659 69666 69638 69579 70119 70134 70136 70142 70144 70145 70146 70147 70148 70162 70167 70169 70172 70173 70174 70175 70143 S25610 S25720 S25725 S25729 S69776 S69785 S70157 S70160 S70165 S70176 S70192 S70203 S70206 S70207 S70208 S70209 S70210 S70211 S70129 S70177 S70181 S70205 S70114 S70115 S70117 S70118 S70120 S70121 S70124 S70125 S70126 S70127 S70128 S70130 S70131 S70132 S70138 S70139 S70140 S70163 S70164 S70166 S70182 S70183 S70185 S70187 S70188 S70190 S70191 S701 |
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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-0525-2021%22
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