GETINGE recalls Maquet Servo-I Ventilator Edi Catheter with incorrect expiry date on single packs. This may lead to improper use of the catheter for monitoring diaphragm activity or feeding. Contact for replacement or return.
Edi Catheter labeled with wrong expiry date on single pack EDI catheter boxes
GETINGE is recalling Maquet Servo-I Ventilator Edi Catheters that have an incorrect expiry date on the single-use packaging. This could lead to improper use of the catheter for monitoring diaphragm activity or feeding, potentially causing medical issues.
The Edi Catheter is a single-use medical device for detecting diaphragm electrical activity and administering nutrition. If the expiry date is incorrect, the catheter may be used after its expiration date, potentially causing medical complications.
Healthcare professionals using the Maquet Servo-I Ventilator Edi Catheters for medical monitoring or feeding. Patients receiving care through these catheters are at risk if the incorrect expiry date leads to improper use.
Check for the product code 6685775 on the packaging. The Edi Catheter is a single-use naso-gastric feeding tube with an electrode array. The lot number 92265355 and UDI code 6685775: 07325710002100 are associated with this recall.
Verify the expiry date on the single-pack Edi Catheter packaging to ensure it matches the correct date.
The Edi Catheter has an incorrect expiry date on the single-pack packaging, which could lead to improper use of the catheter for monitoring diaphragm activity or feeding.
The recall record does not specify a remedy, so contact GETINGE directly for guidance.
The recall indicates a potential risk due to the incorrect expiry date, but the product is not inherently unsafe if used correctly.
We’ve drafted a message you can send GETINGE to request your refund or repair — edit it as you like.
Subject: Recall Z-1221-2019 — GETINGE GETINGE Hello, I own a GETINGE that is covered by recall Z-1221-2019 from GETINGE. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
