HIGH

Steris Washers Recalled Due to Electrical Arcing Hazard

Steris recalled 22 AMSCO 7053HP Washer/Disinfectors on November 19, 2025, due to a risk of electrical arcing. The issue arises from a wire connected to the electrical box that may shift from its intended position. Users must stop using the device immediately and follow recall instructions.

Quick Facts at a Glance

Recall Date
November 19, 2025
Hazard Level
HIGH
Brand
Steris
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users).

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Steris Corporation or your healthcare provider for instructions. Notification method: Letter

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Product Details

The recalled AMSCO 7053HP Washer/Disinfector is designed for cleaning and disinfecting hard-surfaced surgical instruments and similar items. The affected model number is 7053HP, with lot codes including UDI: 00724995176662 and various serial numbers. These units were distributed worldwide, including states across the U.S. and Australia.

The Hazard

The wire connected to the electrical box can shift, leading to potential electrical arcing. This arcing remains contained within the unit, posing no shock risk to users but could lead to equipment malfunction.

Reported Incidents

No injuries or incidents have been reported in connection with this recall. The defect poses a high hazard level, classified as Class II by the FDA.

What to Do

Stop using the AMSCO 7053HP Washer/Disinfector immediately. Contact Steris Corporation or your healthcare provider for further instructions. Follow the recall notification letter for detailed actions.

Contact Information

For more information, contact Steris Corporation at their official website or call their customer service.

Key Facts

  • Quantity recalled: 22 units
  • Distribution: U.S. states and Australia
  • No injuries reported
  • Electrical hazard from wire shifting

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
ELECTRICAL

Product Classification

Product Details

Brand
Model Numbers
Lot Code: UDI: 00724995176662
00724995176679
00724995176655 Serial numbers of distributed units: 3619725008
3619725011
3619725013
+15 more
Affected States
ALL
Report Date
December 17, 2025
Source Agency
FDA - Medical Devices
Recall Status
ACTIVE

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