NEOMED Pharmacy Syringes (Avanos) – Expiration Date Omission (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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 Amber NonSterile, Product Code BA-S20EO; e. 35mL Oral Syringe Amber NonSterile, Product Code BA-S35EO; f. 3mL Oral Syringe Amber NonSterile, Product Code BA-S3EO; g. 60mL Oral Syringe Amber NonSterile,
Brand
Avanos Medical, Inc.
Lot Codes / Batch Numbers
a. UDIDI 00350770002798, all lot numbers, b. UDIDI 00350770002835, all lot numbers, c. UDIDI 00350770002804, all lot numbers, d. UDIDI 00350770002842, all lot numbers, e. UDIDI 00350770002859, all lot numbers, f. UDIDI 00350770002811, all lot numbers, g. UDIDI 00350770002866, all lot numbers, h. UDIDI 00350770002828, all lot numbers
Products Sold
a. UDIDI 00350770002798, all lot numbers; b. UDIDI 00350770002835, all lot numbers; c. UDIDI 00350770002804, all lot numbers; d. UDIDI 00350770002842, all lot numbers; e. UDIDI 00350770002859, all lot numbers; f. UDIDI 00350770002811, all lot numbers; g. UDIDI 00350770002866, all lot numbers; h. UDIDI 00350770002828, all lot numbers;
Avanos Medical, Inc. is recalling NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product descriptions: a. 0.5mL Oral due to The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.
Recommended Action
Per FDA guidance
Avanos notified consignees via email or overnight FedEx on or about 03/04/2024. Consignees were instructed to locate affected product in their inventories by comparing the case packaging as demonstrated in the letters, and destroying it. An acknowledgment form was provided in order for them to record their inventory, and confirm destruction, to be returned to fieldactioncare@avanos.com. Replacement with unaffected Avanos NeoMed* Pharmacy Syringes Nonsterile (Non ENFit) will be provided to end users who report affected inventory. Distributors are asked to identify their affected customers and provide notification to them, as well as report theirs and their customers inventory to Avanos via the acknowledgment form.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026