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Cook Inc. recalls Percutaneous Gastrojejunostomy Set Product Usage: Intended for the percutaneous placement of a catheter for gastro
Recalled March 7, 2018 · FDA recall Z-0831-2018 · Cook
Hazard
Cook has identified that the affected lots may contain wire guides that were loaded backwards into the wire guide holder. · FDA Class II
Units
Quantities co-mingled into line 1
Sold at
US Nationwide Distribution
Description
Cook has identified that the affected lots may contain wire guides that were loaded backwards into the wire guide holder.
Product
Percutaneous Gastrojejunostomy Set Product Usage: Intended for the percutaneous placement of a catheter for gastroenteric feeding
Manufacturer(s)
Cook Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →