Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1891-2017 — DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND; INTERNAL CODE NUMBER: 0185TR- 0185NA- 018SND 0185NA 0185ND

U.S. FDA — Device Enforcement · France · 2017-04-05 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1891-2017
Date of alert
2017-04-05
Country / jurisdiction
France
Risk level
Class II
Risk type
recall
Brand
PEROUSE MEDICAL
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
15055430
Reported risk: Complaints regarding broken blister.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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