Class I

Medical Device Recall: Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B. Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules

Medical Action Industries, Inc. 306 · July 23, 2026

Reason for Recall

Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.

Distribution

US distribution to states of: IA, VA, MO, KS, FL, OH and LS.

States Affected

FL, IA, KS, MO, OH, VA

Quantity Affected

3,606

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3107-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.