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FDA · Medical devices ·

Kit recall

Medical Action Industries, Inc. 306 recalled Kit on September 16, 2026 because of kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility. It was sold in IA, VA, MO, KS, FL, OH.

Why it was recalled

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

What's recalled

Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules

Quantity: 1,960

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Medical Action Industries, Inc. 306, Arden, NC
Date
Severity
Class I · most serious
the most serious: the product could cause serious health problems or death.
Where sold
IA, VA, MO, KS, FL, OH
US distribution to states of: IA, VA, MO, KS, FL, OH and LS.
Status
Ongoing
Recall number
Z-3106-2026
Source
U.S. Food and Drug Administration

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