FDAClass I · Medical device · Recall Z-3106-2026 · Recalled September 16, 2026

Kit recall — Medical Action Industries, Inc. 306

Agency report date: September 16, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: Kit
Company / brand: Medical Action Industries
Lot / serial / date codes: UDI-DI: 10809160367414. Lot(Expiration Date): 322200(4/1/2026), 324586(4/1/2026), 327335(4/1/2026), 329618(9/1/2026), 347199(11/1/2026), 337283(11/1/2026), 350354(11/30/2026), 375449(5/31/2027)
Distribution: US distribution to states of: IA, VA, MO, KS, FL, OH and LS.

Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Kit recall status

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-3106-2026
Brand: All Medical Action Industries recalls
Classification: Class I
Units affected: 1,960
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

Kit recall status

Companies & origin

Recalling firm location: Arden, NC, United States
Firm address: 25 Heywood Rd, 28704-9302

Identifying details (verbatim from the notice)

Product codes / lots: UDI-DI: 10809160367414. Lot(Expiration Date): 322200(4/1/2026), 324586(4/1/2026), 327335(4/1/2026), 329618(9/1/2026), 347199(11/1/2026), 337283(11/1/2026), 350354(11/30/2026), 375449(5/31/2027)
Distribution: US distribution to states of: IA, VA, MO, KS, FL, OH and LS.
Firm notified the public via: Letter
FDA event ID: 99613
Recall initiated: July 23, 2026
FDA classified: September 9, 2026
FDA report date: September 16, 2026

More Medical Action Industries recalls

Kit recall — Medical Action Industries, Inc. 306FDA · September 16, 2026
Pack Angiography NCMC 3/Cs BANNER recall — Medical Action Industries, Inc. 306FDA · August 5, 2026
Medical Action Industries Inc recall — Medical Action Industries, Inc. 306FDA · May 13, 2026

Other medical device recalls from around the same time

DuoGlide Short-Term Straight Dialysis Catheter recall — Bard Access Systems, Inc.FDA · September 23, 2026
Power-Trialysis Short-Term Straight Dialysis Catheter recall — Bard Access Systems, Inc.FDA · September 23, 2026
Bravo CF capsule delivery device recall — Given Imaging Ltd.FDA · September 16, 2026
BMC/REACTHEALTH Luna G3 APAP REF LG 3600 recall — BMC Medical Co., Ltd.FDA · August 26, 2026
Boston Scientific ENROUTE Transcarotid Neuroprotection System Plus recall — Boston Scientific CorporationFDA · August 26, 2026

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved October 22, 2026 at 6:00 PM UTC.

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