Pharmacy Plus, Inc. dba Vital Care Compounder recalls Lido/Phenylephrine syringes due to lack of sterility assurance. Products may cause infection if used improperly. Check lot numbers for affected items.
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Vital Care Compounder is recalling Lido/Phenylephrine PF syringes because they were produced without proper sterility assurance. Using these syringes could lead to infections if they are not sterile.
FDA inspections found the syringes were produced without sufficient sterility assurance. This means the products could be contaminated, leading to infections if used in medical procedures.
People who have prescription Lido/Phenylephrine syringes with lot number 65972 from the manufacturer's location in Hattiesburg, MS. Healthcare providers and patients using these syringes for medical purposes are most at risk.
Check for lot number 65972 on the syringe packaging. The products were sold by Vital Care Compounder at 115 S. 40th Ave., Hattiesburg, MS starting from October 27, 2022.
Look for lot number 65972 on the syringe packaging to confirm if it is affected.
FDA inspections found the syringes were produced without sufficient sterility assurance, which could lead to contamination and infection if used.
Check for lot number 65972 on the syringe packaging. The products were sold by Vital Care Compounder at 115 S. 40th Ave., Hattiesburg, MS starting from October 27, 2022.
The recall record does not specify a remedy, so contact the manufacturer for further instructions.
We’ve drafted a message you can send Vital Care Compounder to request your refund or repair — edit it as you like.
Subject: Recall D-0035-2023 — Vital Care Compounder Vital Care Compounder Hello, I own a Vital Care Compounder that is covered by recall D-0035-2023 from Vital Care Compounder. 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.
