Entopsis , Inc.: Medical Device Recall in 2023 - (Recall #: Z-1297-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

PCRopsis Activator: a) 1.5mL, REF 228001; b) 0.5mL,REF 228002; nucleic acid extraction from a variety of biological samples

Product Classification:

Class II

Date Initiated: February 21, 2023

Date Posted: April 5, 2023

Recall Number: Z-1297-2023

Event ID: 91723

Reason for Recall:

Presence of misleading label statements on the product label.

Status: Ongoing

Product Quantity: 52 units

Code Information:

a) REF 282001: Lot Numbers: 3, Exp. 05/2023; 4, Exp. 07/2023; b) REF 228002: Lot Numbers: 3, Exp. 05/2023; 4, Exp. 07/2023; 5, Exp. 04/2023

Distribution Pattern:

Nationwide and Canada, UK, Portugal, England, Spain, England , Germany, Brazil, Denmark, KOR, South Korea, Colombia, Lithuania

Voluntary or Mandated:

Voluntary: Firm initiated