Entopsis recalls PCRopsis Support products with misleading label statements. Affected items include 1mL (REF 787001), 0.25mL (REF 787002), and 25uL (REF 787003) versions. Consumers should check lot numbers and expiration dates.
Presence of misleading label statements on the product label.
Entopsis is recalling three specific PCRopsis Support products due to misleading label statements. This issue could lead to confusion about the product's intended use and potential misuse in laboratory settings.
The product labels contain misleading statements that could cause confusion about the product's intended use. This might lead to incorrect application in laboratory settings, especially when handling biological samples. Misuse could result in improper results or safety issues.
Laboratory users who purchased PCRopsis Support products with the specified reference numbers and expiration dates are affected. Researchers and technicians working with nucleic acid extraction may be at higher risk due to potential misinterpretation of product labels.
Check for the reference numbers: 787001 (1 mL), 787002 (0.25 mL), or 787003 (25 uL). The affected products have specific lot numbers and expiration dates listed in the recall notice.
Review the reference number and lot numbers on your PCRopsis Support product to confirm if it is affected.
The affected products are PCRopsis Support with reference numbers 787001 (1 mL), 787002 (0.25 mL), and 787003 (25 uL).
Check the reference number and lot numbers on your product. If it matches the affected items listed, you may need to contact Entopsis for further instructions.
The recall is due to misleading label statements, which could cause confusion in laboratory use but does not pose a direct safety risk.
We’ve drafted a message you can send Entopsis to request your refund or repair — edit it as you like.
Subject: Recall Z-1301-2023 — Entopsis Entopsis Hello, I own a Entopsis that is covered by recall Z-1301-2023 from Entopsis. 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.
