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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices

Getinge Aquadis 56 Washer Disinfectors Recalled for Premature Pump Wear

Agency Publication Date: May 5, 2025
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Summary

Getinge Disinfection Ab is recalling 526 Aquadis 56 Washer Disinfectors, including models 56A and 56M, because the internal circulation pump may wear out much faster than expected. A programming error causes the pump to start earlier than it should, which leads to premature damage to the pump's seal. While no injuries have been reported, this defect can affect the machine's performance and long-term durability. Owners should stop using the devices and contact the manufacturer or an authorized distributor to arrange for a software correction or repair.

Risk

The internal circulation pump starts prematurely due to a software error, causing the pump's axial seal to wear down early. This could lead to equipment failure or leaks during the disinfection process, potentially compromising the sterilization workflow.

What You Should Do

  1. This recall affects Getinge Aquadis 56 Washer Disinfectors, Model numbers 56A and 56M, which were distributed worldwide between April 2024 and April 2025.
  2. Identify if your device is affected by checking the model number and serial number located on the device label. Affected units are associated with UDI-DI codes 07340153710344 and 07340153710351. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled washer disinfectors immediately to prevent further wear on the pump components.
  4. Contact Getinge Disinfection Ab or your authorized medical equipment distributor to schedule a correction or repair for the affected units.
  5. Call the FDA's consumer contact line at 1-888-463-6332 (1-888-INFO-FDA) for additional information or questions about this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Washer Disinfector Aquadis 56 (Model 56A)
Variants: Model 56A
Model / REF:
56A
Serial Numbers (102):
WAA104857
WAA107934
WAA107937
WAA108359
WAA108540
WAA108963
WAA109338
WAA110115
WAA108201
WAA109175
WAA109884
WAA109989
WAA109998
WAA110804
WAA600035
WAA109641
WAA109651
WAA111118
WAA106820
WAA106835
WAA106841
WAA107693
WAA107428
WAA107429
WAA600055
WAA600060
WAA600061
WAA106607
WAA106668
WAA106753
WAA107358
WAA109804
WAA106793
WAA108419
WAA110679
WAA109022
WAA109030
WAA109564
WAA109566
WAA109595
WAA109598
WAA105283
WAA107346
WAA600188
WAA107314
WAA107330
WAA110062
WAA110075
WAA110084
WAA110104
UDI:
07340153710344

Recall number Z-1720-2025; 102 units affected (8 US, 94 international).

Product: Washer Disinfector Aquadis 56 (Model 56M)
Variants: Model 56M
Model / REF:
56M
Serial Numbers (424):
WAA105199
WAA105251
WAA105268
WAA105357
WAA105535
WAA105700
WAA105915
WAA105972
WAA105973
WAA106079
WAA106114
WAA106135
WAA106451
WAA106471
WAA106487
WAA106505
WAA107436
WAA107492
WAA107565
WAA107581
WAA107588
WAA107920
WAA108225
WAA108807
WAA108920
WAA108921
WAA108922
WAA109036
WAA109047
WAA109231
WAA109377
WAA109392
WAA109635
WAA109687
WAA109731
WAA109790
WAA109835
WAA109840
WAA109853
WAA109907
WAA109972
WAA110109
WAA110366
WAA110487
WAA110546
WAA110557
WAA110711
WAA110726
WAA110802
WAA110847
UDI:
07340153710351

Recall number Z-1721-2025; 424 units affected (79 US, 345 international).

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96644
Status: Active
Manufacturer: Getinge Disinfection Ab
Sold By: Authorized Medical Equipment Distributors
Manufactured In: Sweden
Units Affected: 2 products (102 units (8 US, 94 OUS); 424 units (79 US, 345 OUS))
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.