FDA recall record

Avanos Medical NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product recall — FDA Z-2035-2024

The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.

Class IIIclassification
Z-2035-2024official record ID
Jun 19, 2024report date

Recall record at a glance

Official recordZ-2035-2024
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusOngoing
Recalling firmAvanos Medical, Inc.
Report dateJun 19, 2024
Recall initiation dateMar 4, 2024
Quantity37,476 cases (16,704,600 units)
LocationAlpharetta, GA, United States

Official product description

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, Product Code BA-S60EO; h. 6mL Oral Syringe Amber NonSterile, Product Code BA-S6EO;

Why the product was recalled

The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.

Distribution information

Worldwide distribution - US Nationwide and the countries of Australia, New Zealand, Canada, Switzerland, Netherlands, Singapore.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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