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Serious recall: Injury is possible or has been reported. Take action promptly.

CooperSurgical, Inc. 2024-12-25 Health serious FDA
Health · FDA · Recall #FDA-Z-0688-2025

Brand Name: K-Systems Product Name: G85 Mini Incubator Model/Catalog Number: K22074 … Recall

Issued December 25, 2024 · CooperSurgical, Inc.

In December 2024, CooperSurgical, Inc. recalled the Brand Name: K-Systems Product Name: G85 Mini Incubator Model/Catalog Number: K22074 …, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will alarm appropriately.

What you should do

  1. 1 Stop using Brand Name: K-Systems Product Name: G85 Mini Incubator Model/Catalog Number: K22074 … right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact CooperSurgical, Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
CooperSurgical, Inc.
Category
Health
Recall date
December 25, 2024
Units affected
Not reported
Sold at
States: NC, NJ, TX, VA, IL, NY, CA, PA Please note: The countries below, excluding Iraq, all consider these devices to be "lab equipment",
Recall number
FDA-Z-0688-2025
Made in
United States
Issuing agency
FDA

In context

  • CooperSurgical, Inc. has 3 recalls in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 737th Health recall we've logged in 2024.
Read the official FDA notice

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