Medtronic recalls DLP Single Stage Venous Cannulae (REF 67312) due to manufacturing error where straight tip models were incorrectly labeled as right angle metal tip. Affected units have specific lot numbers and GTIN.
During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage Venous Cannulae - right angle metal tip (Model 67312).
Medtronic is recalling DLP Single Stage Venous Cannulae with right angle metal tip (REF 67312) because straight tip models were incorrectly labeled as right angle models during manufacturing. This could lead to improper use if the wrong cannula is used in medical procedures.
During manufacturing, straight tip cannulas were incorrectly labeled as right angle metal tip models. This means healthcare providers might use the wrong cannula type, potentially causing improper medical procedures.
Healthcare professionals using these cannulas for medical procedures may be affected. Patients receiving procedures with the recalled cannulas could be at risk if the wrong model is used.
Check for the product label indicating 'DLP Single Stage Venous Cannulae - right angle metal tip (Model 67312)'. Affected units have GTIN 20613994879329 and lot numbers 2023090954 or 202312C065.
Look for the label indicating 'DLP Single Stage Venous Cannulae - right angle metal tip (Model 67312)' on the product.
During manufacturing, straight tip models were incorrectly labeled as right angle metal tip models, which could lead to improper use in medical procedures.
DLP Single Stage Venous Cannulae with right angle metal tip (Model 67312), GTIN 20613994879329, lot numbers 2023090954 and 202312C065.
The recall does not require stopping use; it's a labeling error that could lead to incorrect use if the wrong model is selected.
We’ve drafted a message you can send Medtronic Perfusion Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-3128-2024 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-3128-2024 from Medtronic Perfusion Systems. 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.
