Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE Recalled by PEROUSE MEDICAL Due to Complaints regarding broken blister.
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 PEROUSE MEDICAL directly.
Affected Products
DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND; INTERNAL CODE NUMBER: 0185TR- 0185NA- 018SND 0185NA 0185ND
Quantity: 18,431
Why Was This Recalled?
Complaints regarding broken blister.
Where Was This Sold?
This product was distributed to 3 states: AZ, MN, TN
About PEROUSE MEDICAL
PEROUSE MEDICAL has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report