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Smiths Medical ASD Inc. recalls smiths medical portex Loss of Resistance Device, REF 100/398/000
Recalled October 27, 2021 · FDA recall Z-0152-2022 · Smiths Medical ASD
Hazard
The labeling was missing information on sterilization and prohibition of reuse. · FDA Class II
Units
3420 devices
Sold at
Canada. Belgium, Great Britain, Ireland, Czech Republic, Spain, France, Switzerland, Israel, Germany, Sweden, Italy, New Zealand, Australia, South Africa, Netherlands, Slovenia, United Arab Emirates
Description
The labeling was missing information on sterilization and prohibition of reuse.
Product
smiths medical portex Loss of Resistance Device, REF 100/398/000
Manufacturer(s)
Smiths Medical ASD Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →