Philips recalls autoclavable temperature probes with model numbers 21075A, 21076A, 21078A, 989803162621, 989803162631, 989803162641. The recall involves updated cleaning instructions to prevent improper disinfection.
Update to instructions for use regarding the cleaning and disinfection process for the reusable probes.
Philips is recalling autoclavable temperature probes with specific model numbers due to an update to cleaning instructions. This ensures proper disinfection and prevents potential misuse of the probes.
The recall requires updated cleaning instructions to ensure proper disinfection. Without following the new instructions, the probes could become contaminated or fail to sterilize correctly, potentially leading to infection risks.
Users of Philips autoclavable temperature probes with model numbers 21075A, 21076A, 21078A, 989803162621, 989803162631, or 989803162641 are affected. Healthcare facilities using these probes for temperature monitoring are most at risk.
Check the product packaging for model numbers 21075A, 21076A, 21078A, 989803162621, 989803162631, or 989803162641. The recall applies to all units manufactured from 2008 to present with the specified UDI codes.
Check the product packaging for updated cleaning and disinfection instructions to ensure proper use.
Philips is updating the cleaning instructions to ensure proper disinfection of the probes, which helps prevent contamination.
Models 21075A, 21076A, 21078A, 989803162621, 989803162631, and 989803162641 are affected.
No, the recall does not require stopping use; it only requires following updated cleaning instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0926-2022 — Philips Philips Hello, I own a Philips that is covered by recall Z-0926-2022 from Philips. 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.
