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Insertion Tube Recall: FHC Inc. Removes microTargeting Insertion Tube Sets Due to a Manufacturing Size Error That May Lead to Patient Harm
FHC Inc. is recalling micro Targeting Insertion Tube Sets from a specific product lot after a manufacturing error caused the reducing cannula in these sets to be 20 mm longer than specified.
The FDA has identified this as a Class I recall, the most serious type of recall. This recall involves removing certain devices from where they are used or sold. This device may cause serious injury or death if you continue to use it.
Questions?
Customers in the U.S. with questions about this recall should contact FHC Inc. at 207-666-8190.
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