Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
smiths medical portex Loss of Resistance Device Recalled by Smiths Medical ASD Inc. Due to The labeling was missing information on sterilization and...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Smiths Medical ASD Inc. directly.
Affected Products
smiths medical portex Loss of Resistance Device, REF 100/398/000
Quantity: 3420 devices
Why Was This Recalled?
The labeling was missing information on sterilization and prohibition of reuse.
Where Was This Sold?
Canada. Belgium, Great Britain, Ireland, Czech Republic, Spain, France, Switzerland, Israel, Germany, Sweden, Italy, New Zealand, Australia, South Africa, Netherlands, Slovenia, United Arab Emirates
About Smiths Medical ASD Inc.
Smiths Medical ASD Inc. has 169 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report