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Lower risk Medical device recall · FDA · Published September 14, 2022

Avanos Medical Y-CONNECTOR: No Expiration Date on Sterile Extension Sets

Avanos Medical recalls sterile extension sets for pain control pumps that lack an expiration date. This may lead to using expired medical tubing, potentially causing infections or complications.

🇺🇸 FDA recall #Z-0195-2023Medical deviceAvanos Medical ›
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Recalling firmAvanos Medical, Inc.5405 Windward Pkwy · Alpharetta, GA 30004-3894
✎ GovInfoNow plain-language explainer

What happened, in plain English

Avanos Medical is recalling sterile extension sets for pain control pumps that were distributed without an expiration date. This could lead to using expired tubing, increasing the risk of infections or complications. Read more at govinfonow.com/recall/60060-avanos-medical-y-connector-no-expiration-date-on-sterile-extension.

Source Summary by GovInfoNow · govinfonow.com/recall/60060-avanos-medical-y-connector-no-expiration-date-on-sterile-extension · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0195-2023

Cite this page

“Avanos Medical Y-CONNECTOR: No Expiration Date on Sterile Extension Sets.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60060-avanos-medical-y-connector-no-expiration-date-on-sterile-extension. Based on FDA recall #Z-0195-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0195-2023%22&limit=1).

Why it’s dangerous

Sterile medical tubing should have an expiration date to ensure it remains safe for use. Without an expiration date, the tubing may become contaminated or ineffective over time, increasing the risk of infections or complications during medical procedures.

Who’s affected

Pain control pump users who have the sterile extension sets labeled as SUMMIT MEDICAL PRODUCTS REF 220227 or MPS Acacia CAT NO BC-006-04 are affected. Patients using these sets for medical procedures are at risk of infection if the tubing expires.

How to tell if you have this one

Check for the label 'SUMMIT MEDICAL PRODUCTS, REF 220227' or 'MPS Acacia CAT NO: BC-006-04' on the extension set. These sets were sold with all lot codes and are used with pain control pumps.

  • Brand
    Avanos Medical
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Expiration Date

    Look for an expiration date on the sterile extension set. If none is present, it is part of the recall.

Where it went and when

Where it was distributed

Distributed in 11 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: yesWIMichigan: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: yesNMKansas: not listedKSArkansas: not listedARTennessee: yesTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA distribution: “US: CA, CO, FL, MI, NM, OH, OR, TN, TX, UT, WI” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Colorado, Florida, Michigan, New Mexico, Ohio, Oregon, Tennessee, Texas, Utah, Wisconsin.

Recall timeline

FDA terminated this recall 12 months after the firm started it.

1. Firm started the recall: Sep 14, 202212. FDA classified it Class II: Nov 7, 202223. Published in FDA’s Enforcement Report: Nov 16, 202234. FDA terminated the recall: Aug 31, 2023420222023
  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-0195-2023 (September 14, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0195-2023 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