Medtronic recalls disposable pressure display sets with model numbers 61000 and 62000 due to potential unsealed sterile packing. Affected units include specific lot numbers and GTINs from March 2023.
Potential for unsealed sterile packing.
Medtronic is recalling disposable pressure display sets that may have unsealed sterile packaging. This could lead to contamination if the sets are used without proper sterility.
The sets may have unsealed sterile packaging, which could allow contamination during use. This poses a risk of infection if the sets are not properly sterilized before use.
Healthcare professionals using these disposable pressure display sets in medical settings. Patients receiving care with these sets are at risk if the packaging is compromised.
Check for model numbers 61000 or 62000 with specific lot numbers listed in the recall notice. The sets are sold with a DLP of 114.3 cm (45 inches).
Identify the model number and lot numbers from the recall notice to confirm if your set is affected.
Model numbers 61000 and 62000 with specific lot numbers listed in the recall notice.
Check for model numbers 61000 or 62000 with lot numbers from the list provided in the recall notice.
The recall notice does not specify a remedy.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-1802-2024 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-1802-2024 from Medtronic. 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.
