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Lower risk Medical device recall · FDA · Published October 12, 2022

Medical Action Industries Disposable Scissors Recall: Debris in Scissors

Recall of 20-pack disposable scissors with debris. Stop using if you have these sterile medical instruments.

🇺🇸 FDA recall #Z-0765-2023Medical deviceMedical Action Industries ›
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Recalling firmMedical Action Industries, Inc. 30625 Heywood Rd · Arden, NC 28704-9302
✎ GovInfoNow plain-language explainer

Medical Action Industries recalled disposable scissors that contain debris. This could lead to contamination during medical procedures. Read more at govinfonow.com/recall/59924-medical-action-industries-disposable-scissors-recall-debris-in-scissors.

Source Summary by GovInfoNow · govinfonow.com/recall/59924-medical-action-industries-disposable-scissors-recall-debris-in-scissors · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0765-2023

Cite this page

“Medical Action Industries Disposable Scissors Recall: Debris in Scissors.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/59924-medical-action-industries-disposable-scissors-recall-debris-in-scissors. Based on FDA recall #Z-0765-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0765-2023%22&limit=1).

The FDA announced on Oct. 12, 2022, that Medical Action Industries Inc. is recalling Disposable Instrument Packs containing Littauer Scissors due to debris hazards. Owners should contact the company for a refund or replacement.

How to tell if you have it

  • Brand: Medical Action Industries
  • Product: Disposable Instrument Pack, Littauer Scissor
  • REF: 56247
  • Lot #: 297668
  • UDI: 10809160003473

The hazard

The recalled scissors contained debris, according to the FDA. The agency classified this as a Class II recall.

Context

GovInfoNow's records show Medical Action Industries has 14 other recalls on record since Dec. 2, 2019. Other recent recalls of similar products include Medline 5.5" Sterile Scissors Recall (Nov. 13, 2025), Medline Convenience Kits Recall (July 10, 2026), and Arrow Medical Drainage Kits Recall (April 21, 2026).

How to tell if you have this one

Check for the model REF 56247, sterile packaging, and the lot number 297668. These scissors were sold in 20 packages per box.

  • Brand
    Medical Action Industries
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check for Debris

    Inspect the scissors for visible debris inside the blades.

Where it went and when

Where it was distributed

Distributed in 8 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: yesINOhio: yesOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “Distribution was made to FL, IL, IN, MA, MD, MO, OH, and VA. There was no foreign/government/military distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida, Illinois, Indiana, Maryland, Massachusetts, Missouri, Ohio, Virginia.

Recall timeline

FDA terminated this recall 2.4 years after the firm started it.

1. Firm started the recall: Oct 12, 202212. FDA classified it Class II: Dec 22, 202223. Published in FDA’s Enforcement Report: Dec 28, 202234. FDA terminated the recall: Feb 19, 2025420222025
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-0765-2023 (October 12, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0765-2023 to see it in context.
  • Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA