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Use caution Medical device recall · FDA · Published November 19, 2025

Steris AMSCO 7052HP Washer/Disinfector Recall: Electrical Arcing Risk

Steris recalls AMSCO 7052HP Washer/Disinfector units with potential internal electrical arcing. The hazard is internal and does not risk user shock. Affected units have specific serial numbers and lot codes.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0909-2026Medical deviceSteris ›
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Contact the company

Recalling firmSteris Corporation5960 Heisley Rd · Mentor, OH 44060-1834
✎ GovInfoNow plain-language explainer

Steris is recalling AMSCO 7052HP Washer/Disinfector units because a wire may shift, causing internal electrical arcing. This could lead to fire or damage but does not pose a shock risk to users. The recall affects healthcare facilities using these units. Read more at govinfonow.com/recall/50636-steris-amsco-7052hp-washer-disinfector-recall-electrical-arcing-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/50636-steris-amsco-7052hp-washer-disinfector-recall-electrical-arcing-risk · Updated August 18, 2026 · FDA enforcement record: FDA #Z-0909-2026

Cite this page

“Steris AMSCO 7052HP Washer/Disinfector Recall: Electrical Arcing Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/50636-steris-amsco-7052hp-washer-disinfector-recall-electrical-arcing-risk. Based on FDA recall #Z-0909-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0909-2026%22&limit=1).

The FDA announced on Nov. 19, 2025, that Steris Corporation is voluntarily recalling the AMSCO 7052HP Washer/Disinfector due to a potential electrical arcing hazard. The agency stated the risk remains internal within the unit.

How to tell if you have it

  • Brand: Steris
  • Product: AMSCO 7052HP Washer/Disinfector
  • Model/Catalog Number: 7052HP
  • Lot Code (UDI): 00724995176587, 00724995176594, 00724995176570
  • Serial Numbers: 3619625011, 3621625009, 3621625012, 3621925006, 3621925009, 3622425006, 3622725007, 3623425005, 3623825002, 3624525002
  • Quantity: 10 units
  • Distribution: US states (Arizona, Colorado, Florida, Georgia, Illinois, Kentucky, Louisiana, Michigan, New Hampshire, New York, North Carolina, Pennsylvania, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin) and Australia

The hazard

According to the FDA, a wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. The agency noted that electrical arcing remains internal within the unit.

Context

GovInfoNow's records show Steris Corporation has 29 other recalls on record since June 15, 2017. Recent similar product recalls include the Philips Allura Xper FD10C Medical System Recall (Dec. 15, 2025) and the Philips Allura Xper FD10F Medical System Recall (Dec. 15, 2025), both citing risks of electrical short-circuits.

How to tell if you have this one

Check for serial numbers: 3619625011, 3621625009, 3621625012, 3621925006, 3621925009, 3622425006, 3622725007, 3623425005, 3623825002, 3624525002. Lot codes: UDI:00724995176587, 00724995176594, 00724995176570.

  • Brand
    Steris
  • Category
    Medical device
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    Worldwide - US Nationwide distribution in the states of Arizona, Colorado, Florida, Georgia, Illinois, Kentucky, Louisiana, Michigan, New Hampshire, New York, North Carolina, Pennsylvania, Tennessee, Texas, Utah, Victoria, Virginia, Washington, Wisconsin and the countries of Australia.
Recall numberProduct, codes & lotsQuantity
Z-0909-2026AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description: The AMSCO 7052HP Washer/Disinfector is intended for use in the cleaning and intermediate-level disinfection of soiled reusable simple hard-surfaced rigid surgical instruments (such as forceps and clamps), utensils (such as bedpans, urinals, trays, bowl, basin and kidney dishes), rubber and plastic goods, theatre shoes and other similar and related articles found in healthcare facilities.; Lot Code: UDI:00724995176587, 00724995176594, 00724995176570 Serial number of distributed units: 3619625011, 3621625009, 3621625012, 3621925006, 3621925009, 3622425006, 3622725007, 3623425005, 3623825002, 362452500210
Z-0910-2026AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product Description: The AMSCO 7053HP Washer/Disinfector is intended for use in the cleaning and intermediate-level disinfection of soiled reusable simple hard-surfaced rigid surgical instruments (such as forceps and clamps), utensils (such as bedpans, urinals, trays, bowl, basin and kidney dishes), rubber and plastic goods, theatre shoes and other similar and related articles found in healthcare facilities.; Lot Code: UDI: 00724995176662, 00724995176679, 00724995176655 Serial numbers of distributed units: 3619725008, 3619725011, 3619725013, 3621625010, 3621625011, 3621625013, 3621625014, 3621625015, 3621925001, 3621925002, 3621925005, 3621925010, 3622425005, 3622725005, 3622725011, 3622725012, 3623125006, 3623425016, 3623825008, 3624025002, 3624025008, 362452500722
Based on the official FDA remedy

What to do — step by step

  1. Check Serial Numbers

    Look for serial numbers: 3619625011, 3621625009, 3621625012, 3621925006, 3621925009, 3622425006, 3622725007, 3623425005, 3623825002, 3624525002.

  2. Check Lot Codes

    Look for lot codes: UDI:00724995176587, 00724995176594, 00724995176570.

Where it went and when

Where it was distributed

Distributed nationwide and abroad; the notice names 18 states.

Alaska: nationwideAKMaine: nationwideMEVermont: nationwideVTNew Hampshire: named in the noticeNHWashington: named in the noticeWAIdaho: nationwideIDMontana: nationwideMTNorth Dakota: nationwideNDMinnesota: nationwideMNIllinois: named in the noticeILWisconsin: named in the noticeWIMichigan: named in the noticeMINew York: named in the noticeNYRhode Island: nationwideRIMassachusetts: nationwideMAOregon: nationwideORNevada: nationwideNVWyoming: nationwideWYSouth Dakota: nationwideSDIowa: nationwideIAIndiana: nationwideINOhio: nationwideOHPennsylvania: named in the noticePANew Jersey: nationwideNJConnecticut: nationwideCTCalifornia: nationwideCAUtah: named in the noticeUTColorado: named in the noticeCONebraska: nationwideNEMissouri: nationwideMOKentucky: named in the noticeKYWest Virginia: nationwideWVVirginia: named in the noticeVAMaryland: nationwideMDDelaware: nationwideDEArizona: named in the noticeAZNew Mexico: nationwideNMKansas: nationwideKSArkansas: nationwideARTennessee: named in the noticeTNNorth Carolina: named in the noticeNCSouth Carolina: nationwideSCDistrict of Columbia: nationwideDCOklahoma: nationwideOKLouisiana: named in the noticeLAMississippi: nationwideMSAlabama: nationwideALGeorgia: named in the noticeGAHawaii: nationwideHITexas: named in the noticeTXFlorida: named in the noticeFL

FDA distribution: “Worldwide - US Nationwide distribution in the states of Arizona, Colorado, Florida, Georgia, Illinois, Kentucky, Louisiana, Michigan, New Hampshire, New York, North Carolina, Pennsylvania, Tennessee, Texas, Utah, Victoria, Virginia,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Arizona, Colorado, Florida, Georgia, Illinois, Kentucky, Louisiana, Michigan, New Hampshire, New York, North Carolina, Pennsylvania, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin.

Recall timeline

FDA published this recall 28 days after the firm started it.

1. Firm started the recall: Nov 19, 202512. FDA classified it Class II: Dec 11, 202523. Published in FDA’s Enforcement Report: Dec 17, 202532025
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

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

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

What should I do if I have this product?

Check the serial numbers and lot codes against the provided list to determine if your unit is affected. If affected, contact Steris for further instructions.

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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-0909-2026 (November 19, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0909-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 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