3M recalls specific lots of Attest Super Rapid Readout Steam Challenge Packs that may have caps melting during steam sterilization cycles, potentially causing safety issues. Affected units include model 1496V with lot codes 33P4NJ and 33P56T.
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 Steam Challenge Packs (model 1496V) that may have biological indicator caps melting during steam sterilization cycles. This could lead to improper sterilization and potential safety risks in medical settings.
The biological indicator caps in these specific lots may melt, deform, or crack after a steam sterilization cycle at 132°C or 135°C. This could cause the indicator to fail, leading to improper sterilization of medical equipment and potential safety hazards.
Healthcare facilities using the recalled steam challenge packs for sterilization processes are most at risk. Users should check if their facility has the specific lot codes mentioned.
Check for the model number 1496V on the pack. Look for lot codes 33P4NJ (expires 01/01/2025) or 33P56T (expires 01/02/2025) on the packaging.
Look for lot codes 33P4NJ or 33P56T on the packaging of the Attest Super Rapid Readout Steam Challenge Pack (model 1496V).
The specific lots of 3M Attest Super Rapid Readout Steam Challenge Packs (model 1496V) may have biological indicator caps that melt, deform, or crack during steam sterilization cycles at 132°C or 135°C, potentially causing improper sterilization.
Check the lot code on the packaging. If it matches 33P4NJ (expires 01/01/2025) or 33P56T (expires 01/02/2025), contact 3M for instructions on how to handle the product.
The recall is due to potential failure of the biological indicator during sterilization, which could lead to improper sterilization of medical equipment. However, the product itself does not pose a direct injury risk during normal use.
We’ve drafted a message you can send 3M to request your refund or repair — edit it as you like.
Subject: Recall Z-2638-2023 — 3M 3M Hello, I own a 3M that is covered by recall Z-2638-2023 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.
