Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Delta Vaporizer An anesthetic vaporizer is a device used to Recalled by Penlon, Ltd. Due to It has come to Penlon Ltd's attention of...
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 Penlon, Ltd. directly.
Affected Products
Delta Vaporizer An anesthetic vaporizer is a device used to vaporize liquid anesthetic and deliver a controlled amount of the vapor to the patient.
Quantity: 9208 (of which 576 were within the US)
Why Was This Recalled?
It has come to Penlon Ltd's attention of an instance where the installation and pre-use checks listed in the User Manual may not have been followed prior to the clinical use of the vaporizer. Penlon Ltd has updated the Installation and daily Pre-Use Check sections of the User Manual to ensure that the instructions are explicit and clear.
Where Was This Sold?
This product was distributed to 10 states: FL, IL, KY, MN, NJ, ND, PA, TN, TX, VA
About Penlon, Ltd.
Penlon, Ltd. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report