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

Recall Z-0119-2019 — McKesson Insulin Syringe 0.3mL 31GX5/16 Item Numbers: 102-SN310C31516P Product Usage: Indication of Use: Injection of U-100 insulin only.

U.S. FDA — Device Enforcement · United States · 2018-09-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0119-2019
Date of alert
2018-09-04
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Cypress Medical Products LLC
Product category
device
Product type
Devices
Reported risk: Small hole at the end of the syringe is impeding suction of liquid.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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