Merete Medical recalls OsteoBridge Intramedullary Diaphysis Segment Fixation nails for humerus that may be mislabeled. Affected units include specific lot numbers with use by dates from June 2025 to July 2025. Consumers should check their product labels for these lot numbers.
Product may be mislabeled.
Merete Medical is recalling OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails for the humerus due to potential mislabeling. This means the product might not match the intended specifications, which could lead to improper use or complications during medical procedures.
The product may be mislabeled, meaning the actual product might not match the intended specifications. This could result in improper surgical application or complications during the procedure. However, the recall does not indicate a risk of injury or serious harm in normal use.
Patients who received these OsteoBridge IDSF nails for humerus fractures are likely affected. Medical professionals using the product for surgical fixation may also be at risk if they have the mislabeled items.
Check the product label for lot numbers such as MS1912994R, MS1811555R, or MS1913023R with use by dates between June 4, 2025 and July 24, 2025. These specific lot numbers were identified in the recall notice.
Look for lot numbers like MS1912994R, MS1811555R, or MS1913023R with use by dates from June 4, 2025 to July 24, 2025.
The product may be mislabeled, which could lead to improper use or complications during medical procedures.
Check the product label for specific lot numbers and use by dates listed in the recall notice. If you have the affected lot numbers, contact Merete Medical for further instructions.
The recall indicates a potential mislabeling issue, but it does not specify a risk of injury or serious harm in normal use.
We’ve drafted a message you can send Merete Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0438-2021 — Merete Medical Merete Medical Hello, I own a Merete Medical that is covered by recall Z-0438-2021 from Merete Medical. 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.
