Medline Convenience Kits recalled for anesthetic quality issues
What this means
Medline Convenience Kits containing Arrow Kits and Sets with Lidocaine and Bupivacaine anesthetic injections were recalled due to quality issues found during an FDA inspection of the supplier. The kits are used for central and arterial line procedures in medical settings. A total of 233 units were distributed nationwide.
- If you received one of the affected Medline Convenience Kits (models ACC011142 or DYNJ8407), do not use the anesthetic injections they contain.
- Contact your Medline representative or the FDA for instructions on returning or disposing of the affected kits.
The agency's original wording
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2454-2026More Medline recalls
- FDA-Device2026-09-23Medline anesthesia L&D kits recalled for fungal contamination risk
- FDA-Device2026-09-23Medline Open Heart Convenience Kit recalled for sterile barrier breach risk
- FDA-Device2026-09-23Medline Convenience Kits recalled for fungal contamination in sterile applicators
- FDA-Device2026-09-09Medline Convenience Kits recalled for potential sterility breach in antiseptic applicators
- FDA-Device2026-09-09Medline Convenience Kits with BD ChloraPrep Clear applicators recalled for contamination risk
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