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Medical Device

Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B. Containing Sodium Chloride Injection, 0.9%, USP

Recall date: 2026-09-16 · Source: FDA_DEVICE
Brand / Firm
Medical Action Industries, Inc. 306
Product
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
Reason for recall
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
Units affected
3,606
Description
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
View official recall notice →