3M recalls specific lots of Attest Super Rapid Readout Biological Indicators that may have a cap melting during steam sterilization cycles, risking improper sterilization of medical equipment.
Specific lots of 3M Attest Super Rapid Readout Biological Indicators (1492V), 3M Attest Super Rapid 5 Steam-Plus Challenge (41482V, 41482VF), and 3M Attest Super Rapid Readout Steam Challenge (1496V) may contain biological indicators with a cap that melts, deforms and/or cracks following a steam sterilization cycle of 132¿C and 135¿C.
3M is recalling specific lots of Attest Super Rapid Readout Biological Indicators that may melt during steam sterilization cycles. This could lead to improper sterilization of medical equipment, potentially causing infections.
The biological indicators' caps may melt, deform, or crack after a steam sterilization cycle at 132°C or 135°C. This can cause the indicators to fail, meaning medical equipment might not be properly sterilized.
Healthcare facilities using these specific lots for sterilization cycles are affected. Staff handling these indicators during steam sterilization are at risk of improper sterilization.
Check for lot codes 33P3X3 (expires 12/29/2024) or 33P4NH (expires 01/01/2025) on the packaging. These indicators are used for steam sterilization cycles in healthcare settings.
Look for lot codes 33P3X3 (expires 12/29/2024) or 33P4NH (expires 01/01/2025) on the packaging.
The cap melting can cause the biological indicator to fail, meaning medical equipment might not be properly sterilized.
Check for lot codes 33P3X3 (expires 12/29/2024) or 33P4NH (expires 01/01/2025) on the packaging.
No, but you should check the lot codes and follow the action steps to ensure proper sterilization.
We’ve drafted a message you can send 3M to request your refund or repair — edit it as you like.
Subject: Recall Z-2637-2023 — 3M 3M Hello, I own a 3M that is covered by recall Z-2637-2023 from 3M. 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.
