Boston Scientific recalls certain batches of MAMBA 135 and MAMBA Flex 135 Microcatheters due to incorrect labeling and packaging. Affected units have specific batch numbers and expiration dates.
The firm initiated a removal of certain batches of MAMBA 135 and MAMBA Flex 135 Microcatheters due to incorrect labeling and packaging.
Boston Scientific is recalling specific batches of MAMBA 135 and MAMBA Flex 135 Microcatheters because they were labeled and packaged incorrectly. This issue could lead to confusion about the product's specifications, but it does not pose a direct safety risk to users.
The microcatheters were packaged with incorrect labels and packaging, which could cause confusion about their specifications. However, this does not involve a physical hazard like injury or malfunction during use.
Healthcare professionals who use these microcatheters in medical procedures may be affected. Patients using these catheters are not at risk due to the labeling issue.
Check for the batch numbers 26578155 or 26578465 and expiration date of January 4, 2023 on the carton. The product is labeled with a specific UPN and GTIN code.
Look for batch numbers 26578155 or 26578465 and expiration date of January 4, 2023 on the carton.
Boston Scientific initiated a recall due to incorrect labeling and packaging of certain batches of MAMBA 135 and MAMBA Flex 135 Microcatheters.
The affected batches have UPN numbers H7493928713500 and H7493928713520, with batch numbers 26578155 and 26578465, and an expiration date of January 4, 2023.
No, the recall is for labeling and packaging issues, not a safety hazard that could cause injury.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-1430-2021 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-1430-2021 from Boston Scientific. 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.
