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

Recall Z-0779-2020 — Medical convenience trays and kits, labeled as: Medical Action Industries, Inc.: ***CVC*** Clear Sequence Change Kit, REF 77070B ***DIALYSIS*** Clear Sequence Change Kit, REF 77068B ***PEDS CVC*** Clear Sequence Change Kit, REF 77190B ***PICC*** Clear Sequence Change Kit, REF 77069B Adult Ce

U.S. FDA — Device Enforcement · United States · 2019-12-02 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0779-2020
Date of alert
2019-12-02
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medical Action Industries, Inc. 306
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
0000250140
Reported risk: The kits contain a bottle of saline solution which may exceed the USP specified pH requirements of 4.5-7.0.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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