Mesa Laboratories recalls SporAmpule Biological Indicator (SPS5-100) lots SPS-696, SPS-697, SPS-698 due to bromocresol purple concentration not meeting specifications. Affected users should contact Mesa Laboratories for details.
The concentration of bromocresol purple in the recalled lots does not conform to specification.
Mesa Laboratories is recalling SporAmpule Biological Indicator catalog number SPS5-100 from specific production lots because the bromocresol purple concentration does not meet required specifications. This issue could affect the accuracy of sterilization processes in medical settings.
The bromocresol purple concentration in the recalled lots is incorrect, which may lead to inaccurate sterilization testing. This could result in medical equipment not being properly sterilized, potentially causing infections.
Users of SporAmpule Biological Indicators in medical sterilization processes are likely affected. Healthcare facilities using the recalled lots are at risk of inaccurate sterilization results.
Check for SporAmpule Biological Indicator catalog number SPS5-100. The affected lots are SPS-696, SPS-697, and SPS-698. This product is sold by Mesa Laboratories Bozeman Manufacturing Facility.
Reach out to Mesa Laboratories for specific instructions on handling the recalled product.
SporAmpule Biological Indicator catalog number SPS5-100 from lots SPS-696, SPS-697, and SPS-698.
The concentration of bromocresol purple in the recalled lots does not conform to specification.
Check for SporAmpule Biological Indicator catalog number SPS5-100 and the specific lots SPS-696, SPS-697, or SPS-698.
We’ve drafted a message you can send Mesa Laboratories to request your refund or repair — edit it as you like.
Subject: Recall Z-1274-2018 — Mesa Laboratories Mesa Laboratories Hello, I own a Mesa Laboratories that is covered by recall Z-1274-2018 from Mesa Laboratories. 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.
