FDA Device recall Z-1511-2024
Power Cords, marketed under the following models: a) CORD,METAL EARTH PIN, 2.5A,250V,2.5M,C7, 714682
- FDA Device
- Class II
- ongoing
- Published 2024-04-17
On 2024-04-17 the FDA classified a Class II recall of Power Cords, marketed under the following models: a) CORD,METAL EARTH PIN, 2.5A,250V,2.5M,C7, 714682 by Baxter Healthcare, citing baxter received reports of an issue related to the construction of the power cord not meeting the insulation rating per country-specific requirements and international electrical….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1511-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-03-26 |
| Published | 2024-04-17 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Baxter Healthcare |
| Distribution | IL, NY |
Product
Power Cords, marketed under the following models: a) CORD,METAL EARTH PIN, 2.5A,250V,2.5M,C7, 714682; b) PLFM CLASS II POWER CORD - AUSTRALIA, 716010; c) PLFM CLASS II POWER CORD - EUROPE, 716012; d) POWER CORD,AUSTRALIA,2.5A,250V,2.5M,C7, 008-0910-00; e) POWER CORD,EUROPEAN,2.5A,250V,2.5M,C7, 008-0912-00; f) LINE CORD (EURO), 4500-402; g) LINE CORD (UK), 4500-404; h) LINE CORD (AUS), 4500-406
Reason
Baxter received reports of an issue related to the construction of the power cord not meeting the insulation rating per country-specific requirements and international electrical standards.
Identifiers
| code_info | a) 714682, UDI/DI 732094121469; b) 716010, UDI/DI 732094119916; c) 716012, UDI/DI 732094119879; d) 008-0910-00, UDI/…a) 714682, UDI/DI 732094121469; b) 716010, UDI/DI 732094119916; c) 716012, UDI/DI 732094119879; d) 008-0910-00, UDI/DI 732094033113; e) 008-0912-00, UDI/DI 732094033106; f) 4500-402, UDI/DI 732094004083; g) 4500-404, UDI/DI 732094004076; h) 4500-406, UDI/DI 732094004069 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1511-2024%22
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