RecallRadar

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

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

AgencyFDA Device
Recall numberZ-1511-2024
ClassificationClass II
Statusongoing
Initiated2024-03-26
Published2024-04-17
Last updated2026-09-13 11:57 UTC
CompanyBaxter Healthcare
DistributionIL, 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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