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

Recall Z-3030-2017 — VersaSafe Plastic Cannula - 11 Gauge, Model 9391-0200 Product Usage: Used with secondary IV sets or syringes with a female luer lock adapter to administer fluid and medications through a needle or catheter inserted into a patients artery or vein.

U.S. FDA — Device Enforcement · United States · 2017-06-30 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-3030-2017
Date of alert: 2017-06-30
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: CareFusion 303, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 1470303001

Reported risk: Punctures in blister packaging that was detected during the packaging process.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Recall Z-3030-2017 — VersaSafe Plastic Cannula - 11 Gauge, Model 9391-0200 Product Usage: Used with secondary IV sets or syringes with a female luer lock adapter to administer fluid and medications through a needle or catheter inserted into a patients artery or vein.

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Recall Z-3030-2017 — VersaSafe Plastic Cannula - 11 Gauge, Model 9391-0200 Product Usage: Used with secondary IV sets or syringes with a female luer lock adapter to administer fluid and medications through a needle or catheter inserted into a patients artery or vein.