Entopsis recalls PCRopsis Lysis Beads with misleading label statements. Affected items include specific tube and gram quantities with reference numbers and expiration dates. Consumers should check their product details to determine if they are affected.
Presence of misleading label statements on the product label.
Entopsis is recalling PCRopsis Lysis Beads due to misleading label statements. This issue could lead to confusion about product specifications, potentially affecting proper use in nucleic acid extraction processes.
The product labels contain misleading information that could cause confusion about the product's specifications. This might lead to incorrect usage or handling, but does not pose a direct safety risk like injury or fire.
Users of PCRopsis Lysis Beads for nucleic acid extraction from biological samples. Laboratory professionals and researchers handling these beads are most at risk due to potential confusion in product labeling.
Check for reference numbers (REF) 597000, 597825, 597850, or 5970025 on the product label. Also, look for specific lot numbers and expiration dates listed in the recall notice.
Review the reference number (REF) and lot numbers on your PCRopsis Lysis Beads to see if they match the recalled items listed in the notice.
Entopsis is recalling PCRopsis Lysis Beads with reference numbers 597000, 597825, 597850, and 5970025, as well as specific lot numbers and expiration dates.
No, the recall is for misleading label statements, not a safety hazard. You can continue using the beads but should check if your product matches the recalled items.
The recall does not require immediate action beyond checking your product details. If you have the recalled items, you can contact Entopsis for further guidance.
We’ve drafted a message you can send Entopsis to request your refund or repair — edit it as you like.
Subject: Recall Z-1298-2023 — Entopsis Entopsis Hello, I own a Entopsis that is covered by recall Z-1298-2023 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.
