Recall of NEOMED nonsterile pharmacy syringes due to missing expiration dates on shipping labels, potentially leading to expired syringes being shipped.
The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.
Avanos Medical is recalling several types of nonsterile pharmacy syringes because the expiration date was not printed on the shipping labels. This could result in expired syringes being sent to customers, which may not be safe for use.
The syringes were shipped without expiration dates on their outer labels, meaning customers might receive syringes that have expired. Expired syringes could be unsafe for use, especially if they are intended for medication administration.
People who own or use the recalled NEOMED pharmacy syringes, particularly those who administer medication at home. The risk is low as the hazard involves expired products rather than immediate safety risks.
Check for syringes with the product codes BA-S05EO through BA-S60EO (0.5mL to 60mL) or lot numbers listed in the recall notice. The syringes are amber in color and nonsterile.
Look for the product code (BA-S05EO to BA-S60EO) or lot numbers (UDIDI 00350770002798 to UDIDI 00350770002866) on the syringe packaging.
The recall states that the expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.
The recall indicates that expired syringes could be unsafe for use, but the specific risk level is low as the hazard involves expired products rather than immediate safety risks.
Check for the product codes (BA-S05EO to BA-S60EO) or lot numbers (UDIDI 00350770002798 to UDIDI 00350770002866) listed in the recall notice.
We’ve drafted a message you can send Avanos Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2035-2024 — Avanos Medical Avanos Medical Hello, I own a Avanos Medical that is covered by recall Z-2035-2024 from Avanos Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
