Lower riskMedical device recall · FDA · Published May 20, 2019
Getinge 86-Series Medical Washer-Disinfector Recall: Inlet Hose Collapse Risk
Getinge 86-Series medical washer-disinfectors with part number S-86662003 may have inlet pump hose that collapses during use, causing poor cleaning. Affected units include specific serial numbers.
Possibility that inlet pump hose of the Washer Disinfector Getinge 86-Series (S-8666, S-8668) might collapse during use result in low water pressure within the circulation system and, in the worst case scenario, can result in the contents of the Washer Disinfector not being cleaned properly after finished process.
Take action
Contact the company
📍Recalling firmMaquet Cardiovascular Us Sales, Llc45 Barbour Pond Dr · Wayne, NJ 07470-2094
“Getinge 86-Series Medical Washer-Disinfector Recall: Inlet Hose Collapse Risk.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/67895-getinge-86-series-medical-washer-disinfector-recall-inlet-hose-collapse. Based on FDA recall #Z-1777-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1777-2019%22&limit=1).
Maquet Cardiovascular Us Sales, Llc recalled Getinge 86-Series Medical Washer-Disinfectors on May 20, 2019, according to the FDA. The agency announced the Class II recall due to a risk of improper cleaning caused by potential inlet pump hose collapse.
How to tell if you have it
Brand: Getinge
Product: 86-Series Medical Washer-Disinfector
Part Number: S-86662003
Serial Numbers: WAA088731, WAA089124, WAA089128, WAA089586
The hazard
The inlet pump hose of the Getinge 86-Series (S-8666, S-8668) might collapse during use, resulting in low water pressure within the circulation system. This can cause the contents of the Washer Disinfector not to be cleaned properly after the finished process.
Context
GovInfoNow's records show Maquet Cardiovascular Us Sales, Llc has 14 other recalls on record since Oct. 25, 2018. Other recent recalls of similar products include Getinge Thoracic Catheter Recall (Aug. 7, 2026) and Steris AMSCO 7052HP Washer/Disinfector Recall (Nov. 19, 2025).
How to tell if you have this one
Check for the part number S-86662003 on the product label. Affected units have serial numbers: WAA088731, WAA089124, WAA089128, or WAA089586.
Brand
Getinge
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
Terminated
Distribution
Worldwide Distribution - US Nationwide GA, IL, IN, MI, NC, OR, PA, VA Foreign: Australia, Canada, China, France, Germany, India, Japan, Korea, Netherlands, Saudi Arabia, South Africa, Sweden, Switzerland, Thailand, Turkey, United Arab Emirates, Ukraine
Recall number
Product, codes & lots
Quantity
Z-1777-2019
Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86662003 Product Usage: Usage: The Getinge 86 Series Medical Washer-Disinfector is designed for use in healthcare facilities and laboratories where reusable items such as instruments, utensils, anesthesia sets, and glassware are handled for decontamination purposes.; Serail Numbers: WAA088731, WAA089124 , WAA089128, WAA089586
4 units
Z-1778-2019
Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86682003 Product Usage: The Getinge 86 Series Medical Washer-Disinfector is designed for use in healthcare facilities and laboratories where reusable items such as instruments, utensils, anesthesia sets, and glassware are handled for decontamination purposes.; Serail Numbers: WAA088623 WAA088625 WAA088637 WAA088639 WAA088686 WAA088775 WAA088776 WAA088777 WAA088819 WAA088825 WAA088866 WAA088894 WAA088917 WAA088948 WAA088949 WAA088950 WAA088951 WAA089058 WAA089060 WAA089123 WAA089137 WAA089138 WAA089141 WAA089143 WAA089201 WAA089247 WAA089251 WAA089262 WAA089269 WAA089295 WAA089298 WAA089323 WAA089327 WAA089334 WAA089337 WAA089350 WAA089363 WAA089416 WAA089436 WAA089649
40 units
Based on the official FDA remedy
What to do — step by step
Check Product Serial Number
Look for the serial numbers WAA088731, WAA089124, WAA089128, or WAA089586 on the device.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 8 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide Distribution - US Nationwide GA, IL, IN, MI, NC, OR, PA, VA Foreign: Australia, Canada, China, France, Germany, India, Japan, Korea, Netherlands, Saudi Arabia, South Africa, Sweden, Switzerland, Thailand, Turkey, United Arab…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Georgia, Illinois, Indiana, Michigan, North Carolina, Oregon, Pennsylvania, Virginia.
Recall timeline
FDA terminated this recall 4.6 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-1777-2019 (May 20, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1777-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 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.