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

Recall Z-1309-2018 — Personal Intermittent Catheters- 16" and 10" lengths - 30 catheters per box, each catheter is packaged in an individual pouch, Item Numbers: 50612, 50614, 50616, 50618, 52306, 52308, 52310, 52606, 52606G, 52608, 52608G, 52610, 52610G, 53314, 53320, 53514G, 53610, 53610G, 53612G, 53614G, 53616G, 5

U.S. FDA — Device Enforcement · United States · 2017-09-14 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1309-2018
Date of alert
2017-09-14
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
C.R. Bard, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
53621355
Reported risk: Several instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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