Entopsis recalls PCRopsis Reagent RVD-RT products with misleading label statements. Affected items include 1mL, 25mL, and 100mL vials with specific lot numbers. Consumers should check their product labels for the listed reference numbers and expiration dates.
Presence of misleading label statements on the product label.
Entopsis is recalling PCRopsis Reagent RVD-RT products due to misleading label statements. This issue could lead to confusion about the product's intended use and expiration dates, potentially affecting lab results.
The product labels contain misleading statements that could cause confusion about the product's expiration dates and intended use. This might lead to incorrect lab procedures or expired reagents being used, but does not pose a direct safety risk to users.
Lab users and healthcare professionals who purchased the PCRopsis Reagent RVD-RT products with the listed reference numbers and expiration dates are most at risk. The recall affects specific lot numbers of the 1mL, 25mL, and 100mL vials.
Check the product label for the reference numbers: 78378001 (1mL), 78378025 (25mL), or 78378100 (100mL). Also look for the specific lot numbers and expiration dates listed in the recall notice.
Look for the reference numbers (78378001, 78378025, or 78378100) and associated lot numbers and expiration dates on the product label.
The affected products are PCRopsis Reagent RVD-RT vials with reference numbers 78378001 (1mL), 78378025 (25mL), and 78378100 (100mL), each with specific lot numbers and expiration dates.
No, the recall is for label statements that could cause confusion, not a safety hazard. You can continue using the products as long as you check the labels for the correct reference numbers and expiration dates.
Check the product label for the reference numbers: 78378001 (1mL), 78378025 (25mL), or 78378100 (100mL), and the specific lot numbers and expiration dates listed in the recall notice.
We’ve drafted a message you can send Entopsis to request your refund or repair — edit it as you like.
Subject: Recall Z-1300-2023 — Entopsis Entopsis Hello, I own a Entopsis that is covered by recall Z-1300-2023 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.
