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

Recall Z-2035-2024 — NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product descriptions: a. 0.5mL Oral Syringe Amber NonSterile, Product Code BA-S05EO; b. 12mL Oral Syringe Amber NonSterile, Product Code BA-S12EO; c. 1mL Oral Syringe Amber NonSterile, Product Code BA-S1EO; d. 20mL Oral Syringe

U.S. FDA — Device Enforcement · United States · 2024-03-04 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2035-2024
Date of alert
2024-03-04
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Avanos Medical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00350770002798
Reported risk: The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.
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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