Cytocell Ltd. 2023-07-26 Health serious FDA
Health · FDA · Recall #FDA-Z-2210-2023
RET Distal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory… Recall
Issued July 26, 2023 · Cytocell Ltd.
In July 2023, Cytocell Ltd. recalled the RET Distal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
DNAs used during the manufacture of two affected models were accidentally inverted during manufacturing.
What you should do
- 1 Stop using RET Distal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Cytocell Ltd. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Cytocell Ltd.
- Category
- Health
- Recall date
- July 26, 2023
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of CA, FL, OH, & SC.
- Recall number
- FDA-Z-2210-2023
- Made in
- United Kingdom
- Issuing agency
- FDA
In context
- Cytocell Ltd. has 2 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.