Arrow International epidural catheter kits recalled for potentially compromised anesthetic sterility
What this means
Arrow International included anesthetic medications (lidocaine, bupivacaine) and saline from a supplier with quality issues in multiple epidural catheter kits. The supplier's products may not be sterile or effective, and compromised sterility in injectable products can cause serious infection or other life-threatening complications.
- If you use these kits in a medical facility, check your inventory against the affected lot numbers listed in the FDA notice
- Do not use recalled kits; return them to your distributor or Arrow International
- Contact your healthcare provider or facility's pharmacy if you have questions about specific lot numbers
The agency's original wording
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2371-2026Want us to check the next one for you?
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