Fresh Recalls

FDAClass I · Medical device · Recall Z-2007-2026 · Recalled May 13, 2026

Medical Action Industries Inc recall — Medical Action Industries, Inc. 306

Agency report date: May 13, 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
Medical Action Industries Inc
Company / brand
Medical Action Industries
Lot / serial / date codes
UDI:20809160490294/ Lot numbers: 342509, 346066, 338434, 339423, 337365, 335489, 336189, 336789
Distribution
US distribution to state of: AZ OUS: None
Agency product description and boundaries

Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case

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: 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"

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: Medical Action Industries Inc

3. Open the official notice or contact

Official recall ID
Z-2007-2026
Brand
Medical Action Industries
Classification
Class I
Units affected
2030 kits
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

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:20809160490294/ Lot numbers: 342509, 346066, 338434, 339423, 337365, 335489, 336189, 336789
Distribution
US distribution to state of: AZ OUS: None
Firm notified the public via
Letter
FDA event ID
98698
Recall initiated
March 17, 2026
FDA classified
May 6, 2026
FDA report date
May 13, 2026
Verify with the official sources:

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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 September 7, 2026 at 6:00 AM UTC. Record retrieved August 11, 2026 at 6:00 PM UTC.

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