Recall Z-3106-2026— Medical Action Industries, Inc. 306

Name: FDA recall Z-3106-2026
Creator: U.S. Food and Drug Administration
Published: 2026-07-23

Class I · Ongoing

Class I FDA medical device recall by Medical Action Industries, Inc. 306, initiated 2026-07-23. FDA's recall record names no specific 510(k) clearance for this event. Product: Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules. Reason: Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility..

Recalling firm: Medical Action Industries, Inc. 306
Classification: Class I
Status: Ongoing
Initiated: 2026-07-23
Firm location: Arden, NC, United States

Product description

Kit: Epidural/Pain TQC 20/Cs, REF: 82465 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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.