PlainRecalls
FDA Devices Moderate Class II Ongoing

RET Distal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory technique for detecting and locating a specific DNA sequence on a chromosome.

Reported: July 26, 2023 Initiated: May 24, 2023 #Z-2210-2023

Product Description

RET Distal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory technique for detecting and locating a specific DNA sequence on a chromosome.

Reason for Recall

DNAs used during the manufacture of two affected models were accidentally inverted during manufacturing.

Details

Recalling Firm
Cytocell Ltd.
Units Affected
61 units
Distribution
US Nationwide distribution in the states of CA, FL, OH, & SC.
Location
Cambridge, N/A

Frequently Asked Questions

What product was recalled?
RET Distal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory technique for detecting and locating a specific DNA sequence on a chromosome.. Recalled by Cytocell Ltd.. Units affected: 61 units.
Why was this product recalled?
DNAs used during the manufacture of two affected models were accidentally inverted during manufacturing.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 26, 2023. Severity: Moderate. Recall number: Z-2210-2023.