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Epimed International recalls NEO-KATH(TM) Caudal Set, REF 201-2430, Sterile
Recalled August 25, 2021 · FDA recall Z-2313-2021 · Epimed International
Hazard
Potential for stylet to protrude from the distal end of the catheter · FDA Class II
Units
140 units
Sold at
Worldwide distribution, with US distribution to CA, DE, OH, OK, PA, VA, WA, WV. International distribution to Canada and Iran.
Description
Potential for stylet to protrude from the distal end of the catheter
Product
NEO-KATH(TM) Caudal Set, REF 201-2430, Sterile
Manufacturer(s)
Epimed International
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →