FDA recall record

Medical Action Industries, Inc. 306 Kit: Single Shot Epidural 20/Cs, REF: 59553 recall — FDA Z-3107-2026

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

Class Iclassification
Z-3107-2026official record ID
Sep 16, 2026report date

Recall record at a glance

Official recordZ-3107-2026
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmMedical Action Industries, Inc. 306
Report dateSep 16, 2026
Recall initiation dateJul 23, 2026
Quantity3,606
LocationArden, NC, United States

Official product 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

Why the product was recalled

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

Distribution information

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

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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Related recall records

Other records from the same recalling company are shown first when available.

Medical DeviceMay 13, 2026

Medical Action Industries Inc recall — FDA Z-2007-2026

Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"

Class IFDA: OngoingMedical Action Industries, Inc. 306