FDA Device recall Z-0852-2015
GETINGE 46-SERIES Medical Washer-Disinfector, Models 46-4 and 46-5, with PACS 300/350 Control Series with dryer --- Class II, exempt from 5…
- FDA Device
- Class II
- terminated
- Published 2014-12-31
On 2014-12-31 the FDA classified a Class II recall of GETINGE 46-SERIES Medical Washer-Disinfector, Models 46-4 and 46-5, with PACS 300/350 Control Series with dryer --- Class II, exempt from 5… by Getinge Disinfection Ab, citing getinge Disinfection AB received complaints regarding sediment residuals in the manifold of the washer and disinfector of Getinge 46-Series (CM302) with PACS 300/350 control. Afte….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0852-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-11-26 |
| Published | 2014-12-31 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Getinge Disinfection Ab |
| Distribution | US |
Product
GETINGE 46-SERIES Medical Washer-Disinfector, Models 46-4 and 46-5, with PACS 300/350 Control Series with dryer --- Class II, exempt from 510(k) requirements. For use in healthcare facilities and laboratories where reusable items such as instruments, utensils, anesthesia sets, and glassware are handled for decontamination purposes.
Reason
Getinge Disinfection AB received complaints regarding sediment residuals in the manifold of the washer and disinfector of Getinge 46-Series (CM302) with PACS 300/350 control. After performing detailed root cause analysis, the firm has identified the problem as insufficient water flow throughout the manifold due to formation of air pockets where sedimentation may occur.
Identifiers
| code_info | Serial Numbers: SEV0810077, SEV0537108, SEV0633084, W50030454, SEV0724143, SEV0724146, SEV0609110, W50044787, SEV053306…Serial Numbers: SEV0810077, SEV0537108, SEV0633084, W50030454, SEV0724143, SEV0724146, SEV0609110, W50044787, SEV0533068, W50042461, W50023731, W50023732, W50038744, W50028760, SEV0802081, W50015468, W50042473, W50045852, W50048201, W50041156, SEV0911139, SEV0832021, W50031347, SEV0538174, SEV0910190, SEV0734181, W50033518, SEV0802083, W50043877, W50015494, W50047828, SEV0633086, SEV0647025, SEV0650003, SEV0650004, SEV0534069, SEV0617130, W50011492, SEV0538177, W50010176, W50027826, SEV0743108, W50012356, SEV0614021, W50039525, SEV0619121, W50021052, W50025573, W50024233, W50010768, SEV0827061, SEV0738121, SEV0804079, SEV0806117, SEV0820063, SEV0820064, W50041988, SEV0727015, SEV0739202, SEV0906031, SEV0814068, SEV0805187, W50050381, W50050415, SEV0808424, SEV0626127, SEV0645102, SEV0710062, SEV0802086, SEV0815031, SEV0815032, W50027223, W50027224, SEV0826158, W50027541, W50043237, SEV0906032, W50012254, W50038229, W50014011, W50013832, W50012253, W50036280, W50036309, W50048577, SEV0 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0852-2015%22
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