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

Recall Z-0749-2021 — Product Code: K05T-02533, Custom Inflation Kit, Custom K05 Sterile EO, Rx Only, (01)00884450255803 For Angiography/angioplasty. The contents of the kit include surgical drapes, towels, medicine cups, needles, various bowls, pen and label sets (PAL), scalpel, several syringes, table covers, sto

U.S. FDA — Device Enforcement · United States · 2020-11-10 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0749-2021
Date of alert
2020-11-10
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Merit Medical Systems, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00884450255803
Reported risk: Angiography/Angioplasty custom kits contain header bags which may not be fully sealed, resulting in a compromised sterile barrier. This could result in exposure to non-sterile devices which may lead to an infection requiring medical treatment.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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