Technopath recalls Multichem P devices with part code 08P90-10 due to broken glass vials that may expose users to biohazardous material. Affected units include specific lot numbers and models.
Technopath Manufacturing Ltd. has identified an issue with the glass vial commodity used to fill the Multichem S Plus Level 1, Multichem S Plus Level 2, Multichem S Plus Level 3, Multichem IA Plus and Multichem P Controls. Some customers have experienced broken vials when receiving or thawing Technopath Multichem IA Plus and Multichem S Plus Controls. Breakages have been observed upon delivery, while thawing or while opening the vial. The breakages can result in the bottom of the vial breaking off, breakage in the neck thread area or cracking on the sides of the vial. This may expose the user to biohazardous material if cut and may cause a delay in patient results.
Technopath is recalling Multichem P devices because glass vials can break during delivery, thawing, or opening. This breakage may expose users to biohazardous material or delay patient results.
Glass vials can break when received, thawed, or opened, causing pieces to break off the bottom or neck. This may expose users to biohazardous material if cut, potentially delaying patient results.
Users of Multichem P devices with specific lot numbers are affected. Healthcare professionals handling the devices are most at risk due to potential biohazard exposure.
Check for part code 08P90-10, lot numbers 04530621P, 04561021P, or 04610523P on the device. The product is sold as Multichem P controls.
Inspect the vial for cracks, breaks, or pieces that may expose biohazardous material.
Reach out to Technopath Manufacturing Ltd. for specific guidance on affected units.
The vials can break during delivery, thawing, or opening, causing pieces to break off the bottom or neck.
Check for biohazardous material exposure and contact Technopath Manufacturing Ltd. for guidance.
Look for part code 08P90-10 and lot numbers 04530621P, 04561021P, or 04610523P on the device.
We’ve drafted a message you can send Technopath to request your refund or repair — edit it as you like.
Subject: Recall Z-0106-2024 — Technopath Technopath Hello, I own a Technopath that is covered by recall Z-0106-2024 from Technopath. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
